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Anti-Itch

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This product has been discontinued

Active ingredient
Hydrocortisone 1 g/100 g
Other brand names
Dosage form
Spray
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2013
Label revision date
June 19, 2018
Active ingredient
Hydrocortisone 1 g/100 g
Other brand names
Dosage form
Spray
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2013
Label revision date
June 19, 2018
Manufacturer
Car One
Registration number
part348
NDC root
41520-366

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If you are a consumer or patient please visit this version.

Drug Overview

This medication is designed to provide temporary relief from itching caused by minor skin irritations and rashes. You may find it helpful for specific conditions such as eczema, reactions to poison ivy, oak, and sumac, as well as irritations from cosmetics, jewelry, soaps, detergents, and insect bites.

It's important to use this product as directed, and for any other uses, you should consult with a doctor for guidance.

Uses

This product is designed to provide temporary relief from itching caused by minor skin irritations and rashes. You can use it for discomfort related to conditions like eczema, as well as reactions to poison ivy, oak, and sumac. It can also help soothe irritation from cosmetics, jewelry, soaps, detergents, and insect bites.

If you have other uses in mind, it's important to consult with your doctor for advice and supervision.

Dosage and Administration

If you are an adult or a child aged 2 years and older, you can apply the medication to the affected area up to 3 to 4 times a day. Make sure to follow this guideline to ensure the best results.

However, if your child is under 2 years old, it’s important not to use this medication without first consulting a doctor. Always prioritize safety and seek professional advice when it comes to younger children.

What to Avoid

It's important to be aware of specific instructions regarding the use of this medication. While there are no listed contraindications, controlled substance classifications, or risks of abuse or dependence, you should take care if the medication is swallowed. In such a case, seek medical help or contact a Poison Control Center immediately. Your safety is paramount, so please follow these guidelines closely.

Side Effects

You should be aware that this product is for external use only and is flammable, so keep it away from fire or flames. Avoid getting it in your eyes. If your condition worsens, or if symptoms last more than 7 days or return shortly after improvement, stop using the product and consult a doctor before using any other hydrocortisone products. It is not intended for treating diaper rash, and you should also avoid puncturing or incinerating the container, as it is under pressure and should not be stored above 120°F.

Keep this product out of reach of children. If swallowed, seek medical help or contact a Poison Control Center immediately.

Warnings and Precautions

This product is for external use only, so please avoid applying it to any internal areas. It is flammable, so keep it away from fire or flames. Be careful not to let it come into contact with your eyes. If your condition worsens, or if symptoms last more than 7 days or return after clearing up, stop using the product and consult your doctor before trying any other hydrocortisone products.

Do not use this product for diaper rash; instead, speak with your doctor for appropriate treatment. Remember, the contents are under pressure, so do not puncture or incinerate the container, and avoid storing it at temperatures above 120°F. If you accidentally swallow the product, seek medical help or contact a Poison Control Center immediately.

Overdose

If you or someone else has swallowed a medication and you suspect an overdose, it’s important to act quickly. Get medical help immediately or contact a Poison Control Center. They can provide guidance on what to do next.

Signs of an overdose can vary, but they may include unusual symptoms that are not typical for the medication. If you notice any concerning changes in behavior or health, don’t hesitate to seek help. Remember, it’s always better to be safe and get professional advice in these situations.

Pregnancy Use

If you are pregnant or planning to become pregnant, you may be wondering about the safety of using hydrocortisone 1% spray. According to the information available, there are no specific warnings, precautions, or dosage changes required for using this spray during pregnancy. Additionally, the product does not indicate that it is contraindicated (not recommended) for pregnant individuals or that it poses any risk to your developing baby.

As always, it's important to consult with your healthcare provider before using any medication during pregnancy to ensure it is appropriate for your individual situation.

Lactation Use

If you are breastfeeding, you can feel reassured that there are no specific warnings or precautions regarding the use of this product while nursing. Additionally, there is no information available about whether this product is excreted in breast milk or any potential risks to your infant. Always consult with your healthcare provider if you have any concerns or questions about medications while breastfeeding.

Pediatric Use

If your child is under 2 years old, it's important not to use this medication without consulting a doctor first. For children aged 2 years and older, you can apply the medication to the affected area, but make sure to do so no more than 3 to 4 times a day. Always follow these guidelines to ensure your child's safety and well-being.

Geriatric Use

While there is no specific information available about the use of this medication in older adults, it’s important to approach any new treatment with caution. Since older adults may have different health needs and responses to medications, you should always consult with a healthcare provider before starting any new medication. They can help determine the right dosage and monitor for any potential side effects, ensuring that the treatment is safe and effective for you or your loved one.

Renal Impairment

It appears that there is no specific information regarding renal impairment (kidney problems) in the provided text. Therefore, there are no guidelines, dosage adjustments, or monitoring instructions to share for patients with kidney issues. If you have concerns about how your kidney health may affect your treatment, it's important to discuss this with your healthcare provider for personalized advice and recommendations.

Hepatic Impairment

If you have liver problems, it's important to know that there are no specific guidelines or dosage adjustments mentioned for your condition in the available information. This means that the standard recommendations apply, but you should always consult your healthcare provider for personalized advice. They can help determine the best approach for your treatment and monitor your liver function as needed.

Make sure to keep your doctor informed about your liver health, as they may want to conduct regular tests to ensure your safety while using any medication. Your well-being is a priority, so don't hesitate to ask questions or express any concerns you may have.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications you are taking, even if there are no known drug interactions or laboratory test interactions associated with them. This ensures that your treatment plan is safe and effective for your individual health needs.

Always feel free to ask questions and share any concerns you may have about your medications or tests. Your healthcare provider is there to help you understand how to manage your health safely.

Storage and Handling

To ensure the safety and effectiveness of your product, store it in a cool, dry place, avoiding temperatures above 120°F (49°C). It's important to keep the product away from fire or flames, as it is flammable. Additionally, please do not puncture or incinerate the container, as it is under pressure and could pose a safety risk.

When handling the product, always prioritize safety by following these guidelines. Proper storage and careful handling will help you use the product effectively while minimizing any potential hazards.

Additional Information

You should apply this medication topically to the affected area, using it no more than 3 to 4 times a day if you are an adult or a child aged 2 years and older. If your child is under 2 years old, do not use this medication without consulting a doctor first. There are no additional details available regarding laboratory tests, abuse potential, or patient counseling.

FAQ

What is the drug used for?

The drug is indicated for the temporary relief of itching associated with minor skin irritation and rashes, including conditions like eczema and insect bites.

How should I use this drug?

For adults and children 2 years of age and older, apply to the affected area not more than 3 to 4 times daily. Do not use in children under 2 years of age without consulting a doctor.

Are there any warnings I should be aware of?

Yes, this product is for external use only, is flammable, and should be kept away from fire. Avoid contact with the eyes, and if symptoms persist for more than 7 days, consult a doctor.

Can I use this drug during pregnancy?

There are no specific warnings or contraindications regarding the use of this product during pregnancy mentioned in the provided text.

Is this drug safe for nursing mothers?

The insert does not provide specific warnings or precautions for nursing mothers regarding the use of this product.

What should I do if I accidentally swallow this drug?

If swallowed, get medical help or contact a Poison Control Center immediately.

Are there any contraindications for this drug?

No contraindications are listed for this drug.

What should I do if my condition worsens?

If your condition worsens or symptoms persist for more than 7 days, stop using the product and consult a doctor.

Packaging Info

Below are the non-prescription pack sizes of Anti-Itch (hydrocortisone 1%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Anti-Itch.
Details

Drug Information (PDF)

This file contains official product information for Anti-Itch, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

The product is identified by the SPL code 34089-3. No additional specific description details are provided in the available text.

Uses and Indications

This drug is indicated for the temporary relief of itching associated with minor skin irritation and rashes due to various conditions, including eczema, poison ivy, oak, and sumac exposure, as well as reactions to cosmetics, jewelry, soaps, detergents, and insect bites.

Other uses of this product should only be undertaken under the advice and supervision of a healthcare professional.

Dosage and Administration

For adults and children aged 2 years and older, the recommended application is to the affected area not more than 3 to 4 times daily. It is important to ensure that the application is limited to the specified frequency to avoid potential adverse effects.

For children under 2 years of age, the product should not be used without consulting a healthcare professional. It is essential to seek medical advice before administering this treatment to this age group.

Contraindications

There are no specific contraindications listed for this product. However, it is imperative to seek immediate medical assistance or contact a Poison Control Center if the product is swallowed.

Warnings and Precautions

The product is intended for external use only. It is imperative to keep the product away from fire or flame due to its flammable nature.

Healthcare professionals should advise patients to avoid contact with the eyes. In cases where the condition worsens, or if symptoms persist for more than seven days, or if symptoms resolve and then recur within a few days, patients should discontinue use of the product. It is essential that patients do not initiate the use of any other hydrocortisone product without prior consultation with a healthcare provider.

This product is not indicated for the treatment of diaper rash; consultation with a physician is recommended in such cases.

Additionally, the product should not be punctured or incinerated, as it is under pressure. Storage should be maintained at temperatures not exceeding 120°F to ensure safety and efficacy.

In the event of accidental ingestion, immediate medical assistance should be sought, or the local Poison Control Center should be contacted without delay.

Side Effects

Patients using this product should be aware of several important warnings and precautions. The product is intended for external use only and is flammable; therefore, it should be kept away from fire or flame. Contact with the eyes should be avoided. If the condition worsens, or if symptoms persist for more than 7 days or clear up and then recur within a few days, patients are advised to discontinue use and consult a doctor before using any other hydrocortisone product.

This product is not recommended for the treatment of diaper rash, and consultation with a healthcare professional is necessary in such cases. Additionally, patients should not puncture or incinerate the container, as it is under pressure. It is crucial to store the product at temperatures not exceeding 120˚F.

Furthermore, this product should be kept out of reach of children. In the event of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is recommended.

Drug Interactions

No specific drug interactions have been identified for the product. Additionally, there are no known interactions with laboratory tests. Therefore, no dosage adjustments or monitoring recommendations are necessary based on drug or laboratory test interactions.

Packaging & NDC

Below are the non-prescription pack sizes of Anti-Itch (hydrocortisone 1%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Anti-Itch.
Details

Pediatric Use

Pediatric patients under 2 years of age should not use this medication; consultation with a healthcare professional is advised. For adults and children aged 2 years and older, the recommended application is to the affected area no more than 3 to 4 times daily.

Geriatric Use

There is no specific information available regarding the use of this medication in geriatric patients, including dosage adjustments, safety concerns, or special precautions. Healthcare providers should exercise caution when prescribing this medication to elderly patients, as individual responses may vary. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy, given the lack of targeted data for this population.

Pregnancy

Hydrocortisone 1% spray has not been specifically studied in pregnant patients, and there are no warnings, precautions, or dosage modifications indicated for its use during pregnancy. The prescribing information does not state whether the product is contraindicated in pregnancy or presents any risk to the fetus.

Healthcare professionals should consider the potential benefits and risks when prescribing this medication to women of childbearing potential. As with any medication, it is advisable to weigh the necessity of treatment against any potential unknown risks to fetal outcomes.

Lactation

There are no specific warnings or precautions regarding the use of this product by lactating mothers. Additionally, there is no information available about the potential for excretion in breast milk or any associated risks to breastfed infants.

Renal Impairment

There is no information available regarding dosage adjustments, special monitoring, or safety considerations for patients with renal impairment. Healthcare professionals should exercise caution and consider the lack of specific guidance when treating patients with reduced kidney function.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to the use of this medication. Consequently, there are no established dosage adjustments, special monitoring requirements, or precautions outlined for individuals with compromised liver function. It is recommended that healthcare providers exercise caution when prescribing this medication to patients with hepatic impairment, given the lack of data on its safety and efficacy in this population. Regular monitoring of liver function may be prudent in these cases, although specific parameters are not defined in the available information.

Overdosage

In the event of an overdosage, immediate medical assistance is crucial. If the substance is ingested, healthcare professionals should advise patients or caregivers to seek medical help or contact a Poison Control Center without delay.

Prompt intervention is essential to mitigate potential adverse effects associated with overdosage. Symptoms may vary depending on the specific substance involved; therefore, a thorough assessment by a medical professional is recommended to determine the appropriate course of action.

Management procedures may include supportive care and symptomatic treatment, tailored to the individual patient's needs. It is imperative that healthcare providers remain vigilant and prepared to address any complications that may arise from an overdosage scenario.

Nonclinical Toxicology

No teratogenic or non-teratogenic effects have been reported in the available nonclinical studies. Additionally, there is no information regarding animal pharmacology and toxicology. The absence of data limits the assessment of potential risks associated with the compound in these areas.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients that in the event of accidental ingestion, it is crucial to seek medical assistance immediately or contact a Poison Control Center. This prompt action is essential to ensure the safety and well-being of the patient.

Storage and Handling

The product is supplied in a configuration that includes specific National Drug Code (NDC) numbers, which are essential for identification and inventory management.

Storage conditions must be strictly adhered to; the product should not be stored at temperatures exceeding 120˚F. It is imperative to keep the product away from fire or flame due to its flammable nature. Additionally, the container must not be punctured or incinerated, as the contents are under pressure and can pose safety risks if mishandled. Proper handling and storage practices are crucial to ensure safety and product integrity.

Additional Clinical Information

The medication is administered topically, with a recommended application frequency of 3 to 4 times daily for adults and children aged 2 years and older. For children under 2 years of age, it is advised to consult a doctor before use. There is no additional information available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Anti-Itch, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Data Generation & Sources

This page was automatically generated and is maintained by the AllDrugs AI Data-Science Team. It was built from the FDA Structured Product Label (DailyMed) for Anti-Itch, retrieved by a validated AI data-extraction workflow.

All FDA-listed dosage forms and strengths are shown in the Packaging & NDC Codes section above. Regulatory status appears in the Summary Information panel above and was verified in the FDA National Drug Code directory and the NSDE NDC Directory daily file.

Note: an automated daemon monitors NSDE checksums; when the record for this NDC changes, the new file is pulled instantly and this page is refreshed.

No human clinician has reviewed this version.

Learn more in our Editorial Policy

Last AI update:

Primary FDA sources:

Orange Book data shown on this page are limited to Regulatory Status (Rx), Established Pharmacologic Class (EPC), and Mechanism of Action (MoA).

Regulatory data notice: Information on this page is reproduced verbatim from FDA public databases (NSDE, Orange Book, Purple Book, DailyMed SPL). NDA/ANDA drugs are FDA-approved, BLA biologics are FDA-licensed. Inclusion alone does not guarantee current market availability or imply FDA endorsement.

Medical disclaimer: This AI-generated content is provided for educational purposes only and does not constitute medical advice. Always consult a licensed healthcare professional for diagnosis or treatment decisions.