Age Perfecting SPF 15 Sunscreen

Product NDC
11822-2222
11-digit product format
118222222
Labeler code
11822
Product ID
11822-2222_61ce33c3-c000-52bf-e053-2a91aa0a1221
Type
HUMAN OTC DRUG
Nonproprietary name
Ensulizole 1.70% Octinoxate 7.50%
Dosage form
CREAM
Route
TOPICAL
Labeler
Rite Aid
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2016-08-30
Marketing end
0000-00-00
Substance
ENSULIZOLE; OCTINOXATE
Active strength
2 g/100g; g/100g
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11822-2222-32020-01-31C16284748780-19d75b9d0-9c25-f424-e053-dadaa90a57ceDrug Facts