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OTC products · Product label record

Dr. Scholls Blister Pain Relief Complete Kit drug information

LIDOCAINE
Scholl's Wellness Company LLC · TOPICAL

Product NDC: 73469-0486

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameLIDOCAINE
Labeler / manufacturerScholl's Wellness Company LLC
RouteTOPICAL
Drug classDrug class not supplied in source label
Product NDC73469-0486
Label effective date2026-08-19

Official product label reference

Dr. Scholls Blister Pain Relief Complete Kit — Scholl's Wellness Company LLC

This page contains 13 source sections for LIDOCAINE, topical route. Label set 58c2b35c-e1ed-7ea8-e063-6294a90a1494, version 2.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Uses Temporarily relieves pain

Purpose

Purposes External Analgesic
Dosage and administration — label text
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 skin to seal lidocaine patch and 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.
Active ingredient
Active Ingredient Lidocaine 4%
Do not use
Do not use: ■ More than one patch on your body at a time ■ If you have had an allergic reaction to lidocaine or other local anesthetics ■ Do not use in large quantities, particularly over raw surfaces or blistered areas ■ For more than one week without consulting a doctor.
While using this medicine
When using this product: ■ Use only as directed. Read and follow all directions and warnings on this carton
When to stop use and seek help
Stop use and ask a doctor if: ■ condition worsens ■ severe burning sensation, redness, rash or irritation develops ■ symptoms persist for more than 7 days or clear up and occur again within a few days ■ you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied.
Pregnancy or breast feeding
If pregnant or breastfeeding, ask a health care professional before use.
Child safety
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Other safety information
Other Information Store between 20-25°C (68-77°F)
Inactive ingredient
Inactive Ingredients Dihydroxyaluminum Aminoacetate, Edetate Disodium, Glycerin, Kaolin, Methylparaben, Polyacrylic Acid, Polysorbate 80, Propylene Glycol, Propylparaben, Polyvinylpyrrolidone (PVP), Sodium Polyacrylate, Tartaric Acid, Titanium Dioxide, Water/Aqua/Eau
Questions
Questions or Comments 1-866-360-3226

Official sources and product identifiers

RxNorm identifiers: 1737778

Package NDC codes

73469-0486-2, 73557-037-01

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.