SUN ULTIMATE FACE SPF 30

Product NDC
14324-013
11-digit product format
143240013
Labeler code
14324
Product ID
14324-013_a5aee721-bd02-42ee-e053-2a95a90a90c8
Type
HUMAN OTC DRUG
Nonproprietary name
OCTINOXATE, OCTISALATE, HOMOSALATE, AVOBENZONE
Dosage form
CREAM
Route
TOPICAL
Labeler
NAOS
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2018-01-31
Marketing end
2020-10-31
Substance
OCTINOXATE; OCTISALATE; HOMOSALATE; AVOBENZONE
Active strength
70 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record