LBEL

Product NDC
14783-013
11-digit product format
147830013
Labeler code
14783
Product ID
14783-013_40004acb-f09e-4a93-a249-c80242ed8804
Type
HUMAN OTC DRUG
Nonproprietary name
TITANIUM DIOXIDE, OXYBENZONE, ZINC OXIDE, and OCTINOXATE
Dosage form
POWDER
Route
TOPICAL
Labeler
Ventura International, Limited
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2010-12-15
Marketing end
0000-00-00
Substance
TITANIUM DIOXIDE; OXYBENZONE; ZINC OXIDE; OCTINOXATE
Active strength
0 g/g; g/g; g/g; g/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
14783-013-112025-05-06C16284748780-1960f7f55-cb00-8e05-e053-dbdaa90a074a5847df45-8e49-4648-8030-4821d2628108
14783-013-112019-10-29C16284748780-1960f7f55-cb00-8e05-e053-dbdaa90a074a5847df45-8e49-4648-8030-4821d2628108