LOreal Paris Sublime Sun

Product NDC
49967-371
11-digit product format
499670371
Labeler code
49967
Product ID
49967-371_d25ddcee-d093-472a-a843-d004d6445a3c
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone Homosalate Octisalate Octocrylene Oxybenzone
Dosage form
LOTION
Route
TOPICAL
Labeler
L'Oreal USA Products Inc
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2011-10-01
Marketing end
0000-00-00
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Active strength
2 mL/50mL; mL/50mL; mL/50mL; mL/50mL; mL/50mL
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record