Home NDC 76305-302 Aulief
Product NDC 76305-302
11-digit product format 763050302
Labeler code 76305
Product ID 76305-302_42c89af1-c7d8-0ee3-e063-6394a90a3aef
Type HUMAN OTC DRUG
Nonproprietary name Menthol and Camohor
Dosage form CREAM
Route TOPICAL
Labeler China-Gel, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-05-14
Substance CAMPHOR (NATURAL); MENTHOL
Active strength 30; 50 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 Aulief
Brand name suffix Topical Pain Reliever
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (NATURAL) 30 mg/g MENTHOL 50 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination N20HL7Q941 Internal UNII lookup L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1312283 Internal RxNorm lookup 2168358 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 76305-302-01 AuliefTopical Pain Reliever 90.7 g in 1 TUBE CREAM 90.7 4 76305-302-02 AuliefTopical Pain Reliever 198.5 g in 1 TUBE CREAM 198.5 4 76305-302-03 AuliefTopical Pain Reliever 453.6 g in 1 BOTTLE CREAM 453.6 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76305-302 AULIEF TOPICAL PAIN RELIEVER (MENTHOL AND CAMOHOR) CREAM [CHINA-GEL, LLC] 3 Current NDC, Legacy NDC, 3 package rows 20231220_8647dcc3-1dbc-1093-e053-2991aa0a1ab9.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 116 of 152 · 3,029 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 76305-302-01 76305030201 90.7 g in 1 TUBE (76305-302-01) 90.7 g 2019-05-14 0000-00-00 No No Current 76305-302-02 76305030202 198.5 g in 1 TUBE (76305-302-02) 198.5 g 2019-05-14 0000-00-00 No No Current 76305-302-03 76305030203 453.6 g in 1 BOTTLE (76305-302-03) 453.6 g 2019-05-14 0000-00-00 No No Current