LAB SERIES SKINCARE FOR MEN

Product NDC
42472-002
11-digit product format
424720002
Labeler code
42472
Product ID
42472-002_72364155-6a9b-4332-bd81-c02eac31f400
Type
HUMAN OTC DRUG
Nonproprietary name
OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE, and ZINC OXIDE
Dosage form
LIQUID
Route
TOPICAL
Labeler
Aramis Inc.
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2011-04-24
Marketing end
0000-00-00
Substance
OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE
Active strength
74 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42472-002-012020-12-02C16284748780-19d75b9d0-f532-f424-e053-dadaa90a57ce23f3dc49-27cb-4c8b-92a1-4b946655e8a3
42472-002-012020-01-31C16284748780-19d75b9d0-f532-f424-e053-dadaa90a57ce23f3dc49-27cb-4c8b-92a1-4b946655e8a3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
42472-002-01424720002011 BOTTLE in 1 CARTON (42472-002-01) > 50 mL in 1 BOTTLE1 bottle2020-11-190000-00-00NoNoCurrent