FDA.reportPublic FDA data

NU-DERM PHYSICAL UV BLOCK

Product NDC
62032-102
11-digit product format
620320102
Labeler code
62032
Product ID
62032-102_4eac9f57-6759-444e-9182-d01ff3f52155
Type
HUMAN OTC DRUG
Nonproprietary name
ZINC OXIDE
Dosage form
CREAM
Route
TOPICAL
Labeler
OMP, Inc.
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2004-01-01
Marketing end
0000-00-00
Substance
ZINC OXIDE
Active strength
185 mg/g
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62032-102-362019-11-13C16284748780-197449f38-b5be-f6ea-e053-dbdaa90aa703977d55dd-d775-4ed3-9c11-e48652bb194c

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54ZNU-DERM PHYSICAL UV BLOCK SPF 32 (ZINC OXIDE) CREAM [OMP, INC.]1
ZINC OXIDEACTIVE MOIETYSOI2LOH54ZNU-DERM PHYSICAL UV BLOCK SPF 32 (ZINC OXIDE) CREAM [OMP, INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62032-102NU-DERM PHYSICAL UV BLOCK SPF 32 (ZINC OXIDE) CREAM [OMP, INC.]1Legacy NDC20111230_977d55dd-d775-4ed3-9c11-e48652bb194c.zip