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Extra Strength Postpartum Relief

Last content change checked dailysee data sync status

This product has been discontinued

Active ingredient
Lidocaine Hydrochloride 40 mg/1000 mg
Other brand names
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2017
Label revision date
March 31, 2017
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 40 mg/1000 mg
Other brand names
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2017
Label revision date
March 31, 2017
Manufacturer
ridge properties
Registration number
part348
NDC root
69804-044
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info (4 NDCs)
Packaging & NDC Codes (4)

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Drug Overview

It seems that there is no specific drug name or relevant information provided in the bullet list to summarize. Without details about the drug's identity, uses, or mechanism of action, I am unable to create a consumer-friendly summary. If you have specific information about a drug, please share it, and I would be happy to help!

Uses

It seems that there are no specific uses or indications provided for this medication. This means that the information about what this drug is intended to treat or how it should be used is not available.

Additionally, there are no mentions of teratogenic effects (which are harmful effects on a developing fetus) or nonteratogenic effects (which do not affect fetal development). If you have any questions or need further information about this medication, it's best to consult with a healthcare professional.

Dosage and Administration

To ensure you use this medication correctly, it's important to follow the detailed instructions provided in the image titled "Directions.jpg." This image contains all the necessary information regarding how to take or apply the medication, including the specific dosage, method, and frequency.

Make sure to refer to this image for comprehensive guidance, as it will help you understand the best way to use the medication effectively. If you have any questions or need further clarification, don't hesitate to reach out to a healthcare professional.

What to Avoid

You can feel reassured that there are no specific contraindications, controlled substance classifications, or concerns regarding abuse, misuse, or dependence associated with this medication. This means that, based on the available information, there are no particular conditions or risks that would prevent you from using it safely. Always remember to consult with your healthcare provider if you have any questions or concerns about your treatment.

Side Effects

You can feel reassured that there are no specific side effects or adverse reactions listed for this medication. This means that, based on the available information, it is considered to have a favorable safety profile. However, as with any medication, it's always a good idea to discuss any concerns or questions with your healthcare provider. They can provide personalized advice and information tailored to your health needs.

Warnings and Precautions

It appears that there are no specific warnings, precautions, or instructions provided in the information available. However, it's always important to be aware of potential side effects or reactions when taking any medication. If you experience any unusual symptoms or have concerns about your health while using this medication, it’s crucial to stop taking it and consult your doctor for guidance.

Additionally, if you find yourself in a situation where you feel you need immediate medical assistance, don’t hesitate to seek emergency help. Always prioritize your health and safety by staying informed and proactive about your treatment.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While there is no specific information available about the signs of overdose for this medication, general symptoms can include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these signs, or if you are concerned about a possible overdose, seek medical help right away.

In case of an overdose, contacting your local emergency services or going to the nearest hospital is crucial. Always keep the medication packaging with you, as it can help healthcare professionals understand what you've taken. Remember, it's better to be safe and get checked out if you have any doubts about your health.

Pregnancy Use

It is important to know that the safety of lidocaine hydrochloride gel during pregnancy has not been established. Because of potential risks to the developing fetus, it is generally not recommended for use while you are pregnant. If you are pregnant or planning to become pregnant, it is crucial to consult your healthcare provider before using this medication to discuss any potential risks and alternatives. Your health and the health of your baby should always come first.

Lactation Use

If you are breastfeeding, you can feel reassured that there are no specific warnings or recommendations 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

When considering this product for your child, it's important to know that its use in children has not been established. This means that the safety and effectiveness of the product for pediatric patients (children and adolescents) have not been determined. Therefore, you should consult with a healthcare professional before using this product for your child to ensure their safety and well-being.

Geriatric Use

When it comes to using this medication in older adults, there is no specific information available about dosage adjustments, safety concerns, or special precautions. This means that if you or a loved one is an older adult considering this medication, it’s important to consult with a healthcare provider. They can help determine the best approach based on individual health needs and any other medications being taken. Always prioritize open communication with your healthcare team to ensure safe and effective treatment.

Renal Impairment

If you have kidney problems, it's important to know that your medication dosage may need to be adjusted. This is especially true if you have reduced creatinine clearance (a measure of how well your kidneys are filtering waste). You should be closely monitored by your healthcare provider to ensure your treatment is safe and effective.

Before starting any medication, your renal function (how well your kidneys are working) should be tested, and these tests should continue periodically during your treatment. If you have severe renal impairment, special considerations will be necessary to manage your care effectively. Always communicate openly with your healthcare team about your kidney health.

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 treatment is safe and effective for you.

Drug Interactions

It's great to know that there are no known interactions between this medication and other drugs or laboratory tests. However, it's still very important to discuss all medications you are taking, including over-the-counter drugs and supplements, with your healthcare provider. This ensures that your treatment is safe and effective.

Always keep your healthcare provider informed about any changes in your health or new medications you may start. Open communication helps prevent any potential issues and supports your overall well-being.

Storage and Handling

To ensure the best quality and safety of your product, store it at room temperature, away from direct light. It's important to keep the container tightly closed when not in use to prevent contamination. Once you open the container, please remember to discard it after use to maintain safety and effectiveness. Following these guidelines will help you use the product safely and effectively.

Additional Information

No further information is available.

FAQ

What should I do for dosage and administration instructions?

Please refer to the image 'Directions.jpg' for detailed dosage and administration instructions.

Are there any contraindications for this drug?

No contraindications are listed for this drug.

Is this drug safe to use during pregnancy?

Safety during pregnancy has not been established, and use is not recommended due to potential risks to the fetus. Consult your healthcare provider if you are pregnant or planning to become pregnant.

Can this drug be used in pediatric patients?

Pediatric use has not been established, and safety and effectiveness in children have not been determined.

What should I do if I have renal impairment?

If you have renal impairment, dosage adjustments may be necessary, and you should be closely monitored. Renal function tests should be performed prior to and during treatment.

How should I store this drug?

Store at room temperature, protect from light, keep the container tightly closed, and discard after opening.

Are there any specific warnings or side effects associated with this drug?

No specific warnings or side effects are listed in the provided information.

Packaging Info

Below are the non-prescription pack sizes of Extra Strength Postpartum Relief (lidocaine hcl). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Extra Strength Postpartum Relief.
Details

Drug Information (PDF)

This file contains official product information for Extra Strength Postpartum Relief, 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 data.

Uses and Indications

This drug is indicated for use in patients as determined by the prescribing healthcare professional. Currently, there are no specific indications or usage details provided.

There are no known teratogenic or nonteratogenic effects associated with this drug. Healthcare professionals should consider the absence of these effects when evaluating treatment options for their patients.

Dosage and Administration

Healthcare professionals are advised to refer to the image "Directions.jpg" for detailed dosage and administration instructions. This image contains essential information regarding the specific route, method, and frequency of administration. It is crucial to consult this resource to ensure accurate dosing and proper administration techniques.

Contraindications

There are no contraindications associated with the use of this product. It is not classified as a controlled substance, and there are no known risks of abuse, misuse, or dependence. Therefore, no specific instructions regarding avoidance or non-use are necessary.

Warnings and Precautions

The absence of specific warnings, general precautions, laboratory tests, and instructions for emergency medical help or cessation of use indicates a lack of detailed guidance in the provided content. Healthcare professionals are advised to exercise clinical judgment and consider patient-specific factors when prescribing or administering the medication.

It is essential for healthcare providers to remain vigilant for any adverse reactions or complications that may arise during treatment. Regular monitoring of patient responses and any relevant laboratory parameters should be conducted to ensure safe and effective use of the medication.

In the event of any concerning symptoms or adverse effects, healthcare professionals should instruct patients to seek immediate medical attention. Additionally, if a patient experiences significant side effects or if the treatment is no longer deemed appropriate, they should be advised to discontinue use and consult their healthcare provider promptly.

For comprehensive safety information, healthcare professionals should refer to the full prescribing information and consider the latest clinical guidelines relevant to the medication in question.

Side Effects

In the evaluation of adverse reactions associated with the use of this product, no specific side effects have been identified in the warnings section. Furthermore, there are no additional adverse reactions or important notes documented. As such, the safety profile remains unremarkable with respect to reported adverse events. It is essential for healthcare professionals to monitor patients for any unexpected reactions during treatment, as individual responses may vary.

Drug Interactions

No drug interactions or drug and laboratory test interactions have been identified for this product. Therefore, no specific recommendations for dosage adjustments or monitoring are necessary.

Packaging & NDC

Below are the non-prescription pack sizes of Extra Strength Postpartum Relief (lidocaine hcl). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Extra Strength Postpartum Relief.
Details

Pediatric Use

Pediatric use has not been established for this product. Safety and effectiveness in pediatric patients have not been determined.

Geriatric Use

Elderly patients may not have specific information regarding the use of this medication, including dosage adjustments, safety concerns, or special precautions. Therefore, healthcare providers should exercise caution when prescribing this medication to geriatric patients. It is advisable to monitor these patients closely for any adverse effects or changes in therapeutic response, given the lack of targeted data for this population.

Pregnancy

Safety during pregnancy has not been established for lidocaine hydrochloride gel. The use of this medication is not recommended during pregnancy due to potential risks to the fetus. Pregnant patients or those planning to become pregnant should consult a healthcare provider before using this product to discuss potential risks and benefits.

Lactation

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

Renal Impairment

Renal impairment may necessitate dosage adjustments for patients with reduced kidney function. It is essential that patients with reduced creatinine clearance are closely monitored throughout their treatment. Renal function tests should be performed prior to initiation of therapy and periodically during treatment to ensure appropriate management. Special considerations should be taken for patients with severe renal impairment to mitigate potential risks associated with their condition.

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 absence of specific information regarding overdosage, healthcare professionals are advised to exercise caution and adhere to general principles of management in cases of suspected overdose.

It is essential to monitor the patient closely for any potential symptoms that may arise from an overdose. Symptoms can vary widely depending on the substance involved and the individual patient's response.

In the event of an overdose, immediate medical attention should be sought. Healthcare providers should implement supportive care measures, which may include monitoring vital signs, providing symptomatic treatment, and ensuring the patient's safety.

If available, contacting a poison control center or consulting relevant clinical guidelines may provide additional insights into the management of overdose situations.

Overall, vigilance and prompt intervention are critical in managing any suspected overdose effectively.

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 to keep this medication out of reach of children to prevent accidental ingestion or misuse. It is important to emphasize the necessity of proper storage to ensure the safety of young individuals.

Storage and Handling

The product is supplied in a container that must be kept tightly closed to maintain its integrity. It should be stored at room temperature, away from direct light exposure to protect its quality. Once opened, the product should be discarded to ensure safety and efficacy.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Extra Strength Postpartum Relief, 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 Extra Strength Postpartum Relief, 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.