MENTHOL, CAMPHOR

Product NDC
72937-022
11-digit product format
729370022
Labeler code
72937
Product ID
72937-022_4a7f8eec-2023-9c13-e063-6394a90a0c2c
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL, CAMPHOR
Dosage form
CREAM
Route
TOPICAL
Labeler
SUNSET PAIN RELIEF
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-02-12
Substance
CAMPHOR (NATURAL); MENTHOL, UNSPECIFIED FORM
Active strength
3; 10 g/100g; g/100g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
MENTHOL, CAMPHOR
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CAMPHOR (NATURAL)3 g/100g
MENTHOL, UNSPECIFIED FORM10 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiN20HL7Q941, L7T10EIP3A

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72937-022-16MENTHOL, CAMPHOR473 g in 1 JARCREAM4731

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72937-022-1672937002216473 g in 1 JAR (72937-022-16) 473 g2026-02-12NoNoHistorical