Home NDC 0363-9657 Walgreens Kinesiology Pain Relief
Product NDC 0363-9657
11-digit product format 003639657
Labeler code 0363
Product ID 0363-9657_29a68f7b-c375-ff3c-e063-6394a90aca24
Type HUMAN OTC DRUG
Nonproprietary name LIDOCAINE, MENTHOL
Dosage form TAPE
Route TOPICAL
Labeler Walgreen Co.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-11-20
Substance LIDOCAINE; MENTHOL
Active strength 4; 1 mg/100mg; mg/100mg
Pharmacologic classes Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Walgreens Kinesiology Pain Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE 4 mg/100mg MENTHOL 1 mg/100mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 98PI200987 Internal UNII lookup L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1249758 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0363-9657-00 Walgreens Kinesiology Pain Relief 20 in 1 BOX TAPE 20 2 0363-9657-00 Walgreens Kinesiology Pain Relief 1250 mg in 1 APPLICATOR TAPE 1250 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0363-9657 WALGREENS KINESIOLOGY PAIN RELIEF (LIDOCAINE, MENTHOL) TAPE [WALGREEN CO.] 2 Current NDC, 2 package rows 20241222_0fdbb310-8e65-4e0c-b413-a093964324a2.zip
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 18 of 153 · 3,057 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 0363-9657-00 00363965700 20 APPLICATOR in 1 BOX (0363-9657-00) / 1250 mg in 1 APPLICATOR 20 applicator 2024-11-20 No No Current