DIABETIC BRUISE DEFENSE

Product NDC
10738-301
11-digit product format
107380301
Labeler code
10738
Product ID
10738-301_ab7aae57-b41e-4876-aea9-abb52099d04a
Type
HUMAN OTC DRUG
Nonproprietary name
ALLANTOIN
Dosage form
CREAM
Route
TOPICAL
Labeler
Genuine Virgin Aloe Corporation
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2014-01-02
Marketing end
0000-00-00
Substance
ALLANTOIN
Active strength
1 g/100g
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record