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

Additional Listing Data#

Finished product
Yes
Brand name base
Aemerry Numbing Cream
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL2.5 g/50g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A
Rxcui1039690

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87615-002-01Aemerry Numbing Cream50 g in 1 CARTONCREAM501

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1039690menthol 5 % Topical CreamPSN4fefddaf-19c8-86b4-e063-6294a90abffc1
1039690menthol 50 MG/ML Topical CreamSCD4fefddaf-19c8-86b4-e063-6294a90abffc1
1039690menthol 5 % Topical CreamSY4fefddaf-19c8-86b4-e063-6294a90abffc1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
87615-002-018761500020150 g in 1 CARTON (87615-002-01) 50 g2026-05-12NoNoCurrent