Home NDC 87615-002 Aemerry Numbing Cream
Product NDC 87615-002
11-digit product format 876150002
Labeler code 87615
Product ID 87615-002_4fefddaf-19c9-86b4-e063-6294a90abffc
Type HUMAN OTC DRUG
Nonproprietary name Menthol 5%
Dosage form CREAM
Route TOPICAL
Labeler Da Capo Prima LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-05-12
Substance MENTHOL
Active strength 2.5 g/50g
NDC exclude flag No
Listing certified through 2027-12-31
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 Aemerry Numbing Cream
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 2.5 g/50g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 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 1039690 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 87615-002-01 Aemerry Numbing Cream 50 g in 1 CARTON CREAM 50 1
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 111 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 Sample Exclude flag Status 87615-002-01 87615000201 50 g in 1 CARTON (87615-002-01) 50 g 2026-05-12 No No Current