Home NDC 79481-0051 Meijer Pain Relieving
Product NDC 79481-0051
11-digit product format 794810051
Labeler code 79481
Product ID 79481-0051_d7633699-2f24-4365-b436-fc4d79484aec
Type HUMAN OTC DRUG
Nonproprietary name CAMPHOR (SYNTHETIC) and MENTHOL, UNSPECIFIED FORM
Dosage form LOTION
Route TOPICAL
Labeler Meijer Distribution, Inc
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-12-05
Substance CAMPHOR (SYNTHETIC); MENTHOL, UNSPECIFIED FORM
Active strength 55; 160 mg/g; mg/g
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 Meijer Pain Relieving
Brand name suffix analgesic
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (SYNTHETIC) 55 mg/g MENTHOL, UNSPECIFIED FORM 160 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5TJD82A1ET 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 2624710 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 79481-0051-1 Meijer Pain Relievinganalgesic 77 g in 1 TUBE LOTION 77 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79481-0051 MEIJER PAIN RELIEVING ANALGESIC (CAMPHOR (SYNTHETIC) AND MENTHOL, UNSPECIFIED FORM) LOTION [MEIJER DISTRIBUTION, INC] 2 Current NDC, Legacy NDC, 1 package rows 20241116_9953be94-5768-448f-83de-f5e53a2972cc.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 Marketing end Sample Exclude flag Status 79481-0051-1 79481005101 77 g in 1 TUBE (79481-0051-1) 77 g 2022-12-05 0000-00-00 No No Current