Dr. Scholls Blister Pain Relief Complete Kit

LIDOCAINE TOPICAL HUMAN OTC DRUG

Dr. Scholls Blister Pain Relief Complete Kit is an FDA drug label for the active ingredient LIDOCAINE manufactured by Scholl's Wellness Company LLC administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260819.

Generic name
LIDOCAINE
Manufacturer
Scholl's Wellness Company LLC
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
73469-0485
Application
M017
Label effective
20260819

About this product

Dr. Scholls Blister Pain Relief Complete Kit is an FDA-registered drug product whose active ingredient is LIDOCAINE. It is labelled by Scholl's Wellness Company LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 73469-0485, application M017, label effective 20260819. It is one of 152 FDA drug label records sharing the active ingredient LIDOCAINE. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing LIDOCAINE are most often described in connection with: temporarily relieves. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredient Lidocaine 4%

Indications & Usage

Uses Temporarily relieves pain

Dosage & Administration

Directions Adults and children over 12 years: Step 1 (Lidocaine patch application) ■ apply to the affected area not more than 3-4 times daily ■ clean and dry affected area ■ remove backing from lidocaine patch by firmly grasping both ends and gently pulling away backing ■ once exposed portion of patch is positioned, carefully remove remaining backing completely to apply patch to affected area ■ once applied, press firmly on patch to help adhesive adhere to blister ■ do not remove patch and reapply ■ once patch is applied, move to Step 2. Step 2 (Bandage application) ■ remove backing film from hydrogel bandage marked “Step 1” and place center (adhesive side down) over blister ■ remove backing film marked “Step 2” and firmly smooth down adhesive edge to skin to seal lidocaine patch and blister. Replace when bandage begins to loosen Children 12 years or younger : ask a doctor

Warnings

Warnings For external use only ■ Avoid contact with eyes ■ If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor.

More products with the same ingredient

LIDOCAINE

Acolye Numbing Cream Anorectal(Hemorrhoidal) Cream

Guangdong Aimu Biological Technology Co., Ltd View label

Adellina Lidocaine Numbing Cream Topical Anorectal Cream

Guangdong Aimu Biological Technology Co., Ltd View label

Adellina Lidocaine Numbing Cream Topical Anorectal Cream

Guangdong Aimu Biological Technology Co., Ltd View label

AnievaLC

Blackstone Products, LLC View label

Aspercreme Lidocaine XL

Lead Chemical Co., Ltd. View label

Aspercreme with Lidocaine Dry

Chattem, Inc. View label

Assured Bikini Smooth Cream

Zhejiang Jingwei Pharmaceutical Co., Ltd. View label

Bactine Max Antibiotic and Lidocaine Max Pain Relief

WellSpring Pharmaceutical Corporation View label

How products containing LIDOCAINE compare

FDA lists 152 drug label records with LIDOCAINE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

Dosage formProductsManufacturerProducts
— — Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. 10
— — Shanghai Chuangshi Medical Technology (Group) Co., Ltd. 9
— — Proficient Rx LP 6
— — Bryant Ranch Prepack 5
— — Preferred Pharmaceuticals Inc. 5

Frequently asked questions

What is Dr. Scholls Blister Pain Relief Complete Kit used for?
Uses Temporarily relieves pain

Who makes Dr. Scholls Blister Pain Relief Complete Kit?
Scholl's Wellness Company LLC is the labeler of record for Dr. Scholls Blister Pain Relief Complete Kit. 152 FDA label records share the active ingredient LIDOCAINE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Dr. Scholls Blister Pain Relief Complete Kit come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Dr. Scholls Blister Pain Relief Complete Kit prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing LIDOCAINE?
Yes. 152 FDA drug label records list LIDOCAINE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Dr. Scholls Blister Pain Relief Complete Kit been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.