LBel

Product NDC
13537-011
11-digit product format
135370011
Labeler code
13537
Product ID
13537-011_0da5028f-027d-401e-8bbb-cbb5ca204e01
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate and Oxybenzone
Dosage form
LIPSTICK
Route
TOPICAL
Labeler
VENTURA INTERNATIONAL LTD.,
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2010-08-15
Marketing end
0000-00-00
Substance
OCTINOXATE; OXYBENZONE
Active strength
0 g/4g; g/4g
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
13537-011-622025-02-19C16284748780-1956f9ecf-c9c6-621f-e053-dbdaa90a74ad37196036-229e-4061-8379-cf440b15275c
13537-011-622019-10-21C16284748780-1956f9ecf-c9c6-621f-e053-dbdaa90a74ad37196036-229e-4061-8379-cf440b15275c