SPF 50 Signature High Performance Sunscreen

Product NDC
69039-228
11-digit product format
690390228
Labeler code
69039
Product ID
69039-228_896b1f2f-7c0a-41ea-e053-2995a90a55bf
Type
HUMAN OTC DRUG
Nonproprietary name
OCTINOXATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE
Dosage form
LOTION
Route
TOPICAL
Labeler
Sun Bum LLC
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2012-05-03
Marketing end
0000-00-00
Substance
OCTINOXATE; OCTISALATE; OCTOCRYLENE; ZINC OXIDE
Active strength
75 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69039-228-012022-02-06C16284748780-1d6a99b39-503b-a426-e053-dadaa90af4c2896b26b6-a35b-5df7-e053-2995a90adc1a
69039-228-012022-01-28C16284748780-1d6a99b39-503b-a426-e053-dadaa90af4c2896b26b6-a35b-5df7-e053-2995a90adc1a

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69039-228-0169039022801947 mL in 1 BOTTLE (69039-228-01) 947 ml2012-05-030000-00-00NoNoCurrent