Moisture Sunscreen SPF 50

Product NDC
68062-9001
11-digit product format
680629001
Labeler code
68062
Product ID
68062-9001_50b709f4-020b-4c97-e063-6294a90af7c8
Type
HUMAN OTC DRUG
Nonproprietary name
titanium dioxide, zinc oxide
Dosage form
LOTION
Route
TOPICAL
Labeler
Spa de Soleil
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-09-09
Substance
OCTINOXATE; ZINC OXIDE
Active strength
9; 12.6 mg/120mL; mg/120mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Moisture Sunscreen SPF 50
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
OCTINOXATE9 mg/120mL
ZINC OXIDE12.6 mg/120mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii4Y5P7MUD51, SOI2LOH54Z

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68062-9001-12023-01-30C16284748780-1f386c64a-0932-0266-e053-dadaa90a7c1aMoisturizer Sunscreen SPF 50

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68062-9001-1Moisture Sunscreen SPF 50120 mL in 1 TUBELOTION1202

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68062-9001MOISTURE SUNSCREEN SPF 50 (TITANIUM DIOXIDE, ZINC OXIDE) LOTION [SPA DE SOLEIL]1Current NDC, Legacy NDC, 1 package rows20210911_cb95975f-060d-23c2-e053-2a95a90adf1b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68062-9001-168062900101120 mL in 1 TUBE (68062-9001-1) 120 ml2021-09-090000-00-00NoNoCurrent