LBEL

Product NDC
13537-404
11-digit product format
135370404
Labeler code
13537
Product ID
13537-404_7d3d469b-73f4-4516-9a5a-524698888c6f
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Ensulizole, Octisalate, Octocrylene, and Oxybenzone
Dosage form
LOTION
Route
TOPICAL
Labeler
Ventura Corporation Ltd.
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2011-12-13
Marketing end
0000-00-00
Substance
AVOBENZONE; ENSULIZOLE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Active strength
0 g/mL; g/mL; g/mL; g/mL; g/mL
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#