Mineral Ice

Product NDC
0067-2067
11-digit product format
000672067
Labeler code
0067
Product ID
0067-2067_79b588f8-87a3-40c2-8ff6-149e51206e47
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
GEL
Route
TOPICAL
Labeler
GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2011-11-01
Marketing end
2020-08-31
Substance
MENTHOL, UNSPECIFIED FORM
Active strength
0 g/g
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0067-2067-08GM - Gram0067-2067bd6ef823-ad35-4999-8725-01d26374168712012-07-24
0067-2067-16GM - Gram0067-2067f09134d0-87ac-439d-8f0c-2bf447e39f2c12012-07-24
0067-2067-35GM - Gram0067-20671b7c57e4-bc2c-41ef-a5d1-48d3e04544c812012-07-24