Dr. Scholls Blister Pain Relief Complete Kit-8CT

Manufacturer
Scholl's Wellness Company LLC | Shanghai Chuangshi Medical Technology (Group) Co., Ltd.
Effective date
2026-08-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-08-21 02:02:16

Label at a glance#

ProductDr. Scholls Blister Pain Relief Complete Kit
Active ingredientLIDOCAINE
Label structure14 sections

Indications and uses

Temporarily relieves pain

Dosage and administration

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 ...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Purposes

OTC - PURPOSE SECTION

External Analgesic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves pain

Warnings

WARNINGS SECTION

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.

Do not use:

OTC - DO NOT USE SECTION

■ 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
■ On puncture wounds
■ For more than one week without consulting a doctor.

When using this product:

OTC - WHEN USING SECTION

■ Use only as directed. Read and follow all directions and warnings on this carton
■ Avoid contact with eyes and mucous membranes.

Stop use and ask a doctor if:

OTC - STOP USE SECTION

■ 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.

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health care professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION


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

Other Information

OTHER SAFETY INFORMATION

Store between 20-25°C (68-77°F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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 or Comments

OTC - QUESTIONS SECTION

1-866-360-3226

Package label. Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

patchpatch73469-048573469-0485

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130888853003870GTIN-13: 0888853003870
EAN-13: 0888853003870
GTIN-12: 888853003870
UPC-A: 888853003870
GTIN storage (14 digits): 00888853003870
73469-0485.jpg

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73557-03773557-037-01
73469-048573469-0485-8

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-08-06daily-update2026-08-13 01:01:37

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dr. Scholls Blister Pain Relief Complete KitLIDOCAINEScholl's Wellness Company LLC58c2b35c-e1ed-7ea8-e063-6294a90a14942026-08-19WarningsExact identifier
ndc (package): 73557-037-01
ndc11 (package): 73557003701
Dr. Scholls Blister Pain Relief Complete KitLIDOCAINEScholl's Wellness Company LLC585e740b-e4fa-d2aa-e063-6294a90a09822026-08-19WarningsExact identifier
ndc (package): 73469-0485-8
ndc (package): 73557-037-01
ndc (product): 73469-0485
ndc11 (package): 73469048508
ndc11 (package): 73557003701
spl id: 5961b06d-0b71-debc-e063-6294a90a072c
spl set id: 585e740b-e4fa-d2aa-e063-6294a90a0982

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.