FDA.reportPublic FDA data

06 Moisture Foundation SPF 15

Product NDC
57691-112
11-digit product format
576910112
Labeler code
57691
Product ID
57691-112_369e0775-d4c4-404b-bd5a-66c44073b901
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate and Zinc Oxide
Dosage form
EMULSION
Route
TOPICAL
Labeler
The Body Shop Wake Forest
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2009-09-06
Marketing end
0000-00-00
Substance
OCTINOXATE; ZINC OXIDE
Active strength
4 mg/.5mL; mg/.5mL
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57691-112-302020-01-31C16284748780-19d75b9cf-f869-f424-e053-dadaa90a57cemoisture foundation SPF 15

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57691-112-3006 Moisture Foundation SPF 1530 mL in 1 BOTTLE, PUMPEMULSION301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57691-11201 MOISTURE FOUNDATION SPF 15 (OCTINOXATE AND ZINC OXIDE) EMULSION 02 MOISTURE FOUNDATION SPF 15 (OCTINOXATE AND ZINC OXIDE) EMULSION 03 MOISTURE FOUNDATION SPF 15 (OCTINOXATE AND ZINC OXIDE) EMULSION 04 MOISTURE FOUNDATION SPF 15 (OCTINOXATE AND ZINC OXIDE) EMULSION 05 MOISTURE FOUNDATION SPF 15 (OCTINOXATE AND ZINC OXIDE) EMULSION 06 MOISTURE FOUNDATION SPF 15 (OCTINOXATE AND ZINC OXIDE) EMULSION 07 MOISTURE FOUNDATION SPF 15 (OCTINOXATE AND ZINC OXIDE) EMULSION 08 MOISTURE FOUNDATION SPF 15 (OCTINOXATE AND ZINC OXIDE) EMULSION [THE BODY SHOP WAKE FOREST]1Legacy NDC, 1 package rows20100508_90323a05-4f28-4dbd-bd37-26ce0826374d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
57691-112-305769101123030 mL in 1 BOTTLE, PUMP30 mlHistorical