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Super Spot Remover Acne Treatment

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Active ingredient
Salicylic Acid 15 mg/1 mL
Other brand names
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2012
Label revision date
December 15, 2025
Active ingredient
Salicylic Acid 15 mg/1 mL
Other brand names
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2012
Label revision date
December 15, 2025
Manufacturer
ORIGINS NATURAL RESOURCES INC.
Registration number
M006
NDC root
59427-005

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Drug Overview

Super Spot Remover™ is an acne treatment gel designed to help you manage and clear acne blemishes. Its active ingredient, salicylic acid (a compound that helps exfoliate the skin and unclog pores), works to not only clear existing blemishes but also to prevent the development of new ones. With a convenient size of 0.3 fl. oz. (10 ml), this gel can be a helpful addition to your skincare routine if you're looking to improve your skin's appearance.

Uses

If you're dealing with acne, this medication can help manage your condition effectively. It works by clearing existing acne blemishes and also helps prevent the formation of new ones. This means you can expect not only to see improvements in your current skin issues but also to reduce the chances of future breakouts.

Dosage and Administration

Before you start using this medication, make sure to cleanse your skin thoroughly. Once your skin is clean, apply a thin layer of the medication to the entire affected area. You can do this one to three times a day, depending on your needs and your doctor's advice.

It's a good idea to begin with just one application each day to see how your skin reacts. If you find that your skin can handle it, you can gradually increase the frequency to two or three times daily. However, if you experience bothersome dryness or peeling, reduce your application to once a day or even every other day to help your skin adjust.

What to Avoid

It's important to keep this medication out of reach of children. If a child accidentally swallows it, you should call a doctor or contact a Poison Control Center immediately for assistance.

There are no specific contraindications, controlled substance classifications, or noted risks of abuse, misuse, or dependence associated with this medication. However, always use it responsibly and as directed.

Side Effects

It's important to know that this medication is for external use only. You may experience skin irritation and dryness, especially if you are using another topical acne treatment at the same time. To minimize these side effects, it's best to use only one topical acne medication at a time. If you notice any discomfort, consider adjusting your treatment routine.

Warnings and Precautions

This product is intended for external use only, so please avoid applying it to any areas that are not meant for topical treatment. Keep it out of reach of children, and if it is swallowed, seek medical help immediately by calling a doctor or contacting a Poison Control Center.

Be aware that using this product alongside other topical medications can increase the risk of skin irritation and dryness. To minimize these effects, it’s best to use only one topical acne medication at a time. If you experience significant irritation or discomfort, stop using the product and consult your doctor for further advice.

Overdose

If you or someone else has swallowed too much of this medication, it’s important to act quickly. Call your doctor or contact a Poison Control Center immediately for guidance.

Signs of an overdose can vary, but they may include unusual symptoms that require attention. If you notice any concerning changes in behavior or health, don’t hesitate to seek help right away. Your safety is the top priority, so getting prompt medical advice is crucial.

Pregnancy Use

The safety of this product during pregnancy has not been established, so it's important to be cautious. Salicylic acid, a common ingredient in some medications, is contraindicated (not recommended) for use during pregnancy due to potential risks to your developing baby. There is a risk of teratogenic effects, which means it could cause developmental issues in the fetus.

If you are pregnant or planning to become pregnant, you should consult your healthcare provider before using this product. They can help you understand the risks and determine the best options for your health and the health of your baby.

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.

As always, it's a good idea to consult with your healthcare provider if you have any concerns or questions about using any medication while breastfeeding.

Pediatric Use

It's important to keep this medication out of reach of children. If a child accidentally swallows it, you should contact a doctor or call a Poison Control Center immediately for assistance. Taking quick action can help ensure their safety. Always be vigilant about where you store medications to prevent any accidental ingestion.

Geriatric Use

When considering the use of Super Spot Remover Acne Treatment for older adults, it's important to note that the drug insert does not provide specific information about how this product may affect elderly patients. This means there are no special dosage adjustments, safety concerns, or precautions outlined for older individuals.

If you are an older adult or a caregiver, it’s always a good idea to consult with a healthcare professional before starting any new treatment. They can help ensure that the product is appropriate for your specific health needs and circumstances.

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, and there are no special monitoring requirements or precautions outlined for patients with liver impairment.

However, it's always a good idea to discuss your liver health with your healthcare provider before starting any new medication. They can provide personalized advice and ensure that your treatment is safe and effective for you.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. While there are no specific drug interactions or laboratory test interactions noted for this medication, your healthcare provider can help ensure that everything you are taking works well together and is safe for you. Always share your complete list of medications and any recent lab tests to avoid any potential issues. Your health and safety should always come first.

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, be sure to discard any remaining product after use to maintain safety and effectiveness. Following these guidelines will help you use the product safely and effectively.

Additional Information

You should apply this medication topically, covering the entire affected area with a thin layer one to three times a day. It's best to start with one application daily and then gradually increase to two or three times daily if needed or as directed by your doctor. If you experience bothersome dryness or peeling, reduce the application to once a day or every other day.

FAQ

What is Super Spot Remover™?

Super Spot Remover™ is an acne treatment gel that contains 1.5% salicylic acid.

What are the uses of Super Spot Remover™?

It is used for the management of acne, clearing acne blemishes, and helping to prevent the development of new acne blemishes.

How should I apply Super Spot Remover™?

Cleanse your skin thoroughly before applying a thin layer to the affected area one to three times daily. Start with one application daily and gradually increase if needed.

What should I do if I experience dryness or peeling?

If you experience bothersome dryness or peeling, reduce the application to once a day or every other day.

Is Super Spot Remover™ safe to use during pregnancy?

The safety of this product during pregnancy has not been established, and salicylic acid is contraindicated due to potential risks to the fetus.

What precautions should I take when using Super Spot Remover™?

For external use only. Keep out of reach of children, and if swallowed, call a doctor or contact a Poison Control Center immediately.

Are there any known side effects?

Skin irritation and dryness may occur, especially if used with other topical medications. If this happens, use only one topical acne medication at a time.

How should I store Super Spot Remover™?

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

Packaging Info

Below are the non-prescription pack sizes of Super Spot Remover Acne Treatment (salicylic acid). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Super Spot Remover Acne Treatment.
Details

Drug Information (PDF)

This file contains official product information for Super Spot Remover Acne Treatment, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

No description information is available for the specified drug.

Uses and Indications

This drug is indicated for the management of acne. It effectively clears existing acne blemishes and helps prevent the development of new acne blemishes.

There are no teratogenic or nonteratogenic effects associated with this drug.

Dosage and Administration

Healthcare professionals are advised to cleanse the skin thoroughly prior to application. The medication should be applied as a thin layer to cover the entire affected area. Initial dosing should consist of one application daily to minimize the risk of excessive drying of the skin. Based on the patient's response and as directed by a physician, the frequency of application may be gradually increased to two or three times daily.

In cases where bothersome dryness or peeling occurs, it is recommended to reduce the frequency of application to once daily or every other day. Careful monitoring of the patient's skin condition is essential to ensure optimal therapeutic outcomes while minimizing adverse effects.

Contraindications

Use is contraindicated in children due to the risk of accidental ingestion. In the event of swallowing, immediate medical attention should be sought by contacting a doctor or a Poison Control Center.

Warnings and Precautions

For external use only. It is imperative that this product is kept out of reach of children. In the event of accidental ingestion, immediate medical attention should be sought by calling a doctor or contacting a Poison Control Center.

Healthcare professionals should be aware that the concurrent use of this product with other topical medications may increase the risk of skin irritation and dryness. To mitigate this risk, it is recommended that only one topical acne medication be used at a time. Monitoring for signs of skin irritation is advised to ensure patient safety and comfort.

Side Effects

For external use only.

Skin irritation and dryness are common adverse reactions associated with the use of this medication. These reactions are more likely to occur if patients use another topical medication concurrently. To minimize the risk of skin irritation and dryness, it is recommended that patients use only one topical acne medication at a time.

Drug Interactions

There are currently no documented drug interactions associated with this medication. Additionally, there are no known interactions with laboratory tests. As such, no specific recommendations for dosage adjustments or monitoring are warranted at this time.

Packaging & NDC

Below are the non-prescription pack sizes of Super Spot Remover Acne Treatment (salicylic acid). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Super Spot Remover Acne Treatment.
Details

Pediatric Use

Pediatric patients should be advised to keep this medication out of reach of children. In the event of accidental ingestion, it is crucial to contact a healthcare professional or reach out to a Poison Control Center immediately.

Geriatric Use

There is no specific information regarding the use of Super Spot Remover Acne Treatment in geriatric patients. The prescribing information does not provide guidance on dosage adjustments, safety concerns, or special precautions for elderly patients. Therefore, healthcare providers should exercise caution when considering this treatment for patients aged 65 and older, as the absence of data necessitates careful monitoring and individualized assessment of treatment risks and benefits in this population.

Pregnancy

The safety of this product during pregnancy has not been established. Salicylic acid is contraindicated in pregnancy due to potential risks to the fetus, including the risk of teratogenic effects associated with its use. Pregnant women are advised to consult a healthcare provider before using this product to discuss potential risks and alternative options.

Lactation

There are no specific warnings or recommendations regarding the use of this product in nursing 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 prescribing to patients with reduced kidney function.

Hepatic Impairment

There is no information available regarding hepatic impairment, including dosage adjustments, special monitoring, or precautions for patients with compromised liver function. Therefore, no specific recommendations can be made for the use of this medication in patients with hepatic impairment. It is advised that healthcare professionals exercise caution and consider individual patient circumstances when prescribing this medication to patients with liver problems.

Overdosage

In the event of an overdosage, immediate medical attention is crucial. If the substance is ingested, it is imperative to contact a healthcare professional or reach out to a Poison Control Center without delay.

Healthcare providers should be prepared to assess the situation and provide appropriate interventions based on the specific circumstances of the overdosage. Monitoring for potential symptoms associated with the overdosage is essential, as these may vary depending on the substance involved.

Prompt action and thorough evaluation are key components in the management of overdosage cases to ensure patient safety and effective treatment.

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 use of the compound in question.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep the medication out of reach of children to prevent accidental ingestion. It is important to emphasize that if the medication is swallowed, patients should call a doctor or contact a Poison Control Center immediately for assistance. This information is crucial for ensuring the safety and well-being of patients and their families.

Storage and Handling

The product is supplied in a configuration that includes specific NDC numbers, which should be referenced for accurate identification. It is essential to store the product at room temperature to maintain its integrity. Additionally, the product must be protected from light exposure to prevent degradation. The container should be kept tightly closed when not in use to ensure optimal preservation of the contents. It is important to discard the product after opening to ensure safety and efficacy.

Additional Clinical Information

The medication is administered topically, with a recommended application of a thin layer to the entire affected area one to three times daily. Clinicians should advise patients to start with one application per day, gradually increasing to two or three times daily as needed or directed by a healthcare professional. In cases where bothersome dryness or peeling occurs, patients should reduce the frequency of application to once a day or every other day.

No additional information is available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Super Spot Remover Acne Treatment, 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 Super Spot Remover Acne Treatment, 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.

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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.