Private Label SPF45 Water Resistant Paraben Free Sunscreen

Product NDC
60232-0006
11-digit product format
602320006
Labeler code
60232
Product ID
60232-0006_21e18883-f579-425a-a460-1e601e1b30be
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate, Octisalate, Zinc Oxide Sunscreen
Dosage form
LOTION
Route
TOPICAL
Labeler
Swiss-American CDMO, LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2011-08-31
Substance
OCTINOXATE; OCTISALATE; ZINC OXIDE
Active strength
75; 30; 80 g/1000g; g/1000g; g/1000g
Pharmacologic classes
Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Private Label SPF45 Water Resistant Paraben Free Sunscreen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
OCTINOXATE75 g/1000g
OCTISALATE30 g/1000g
ZINC OXIDE80 g/1000g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii4Y5P7MUD51, 4X49Y0596W, SOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60232-0006-1Private Label SPF45 Water Resistant Paraben Free Sunscreen50 g in 1 BOTTLELOTION503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60232-0006PRIVATE LABEL SPF45 WATER RESISTANT PARABEN FREE SUNSCREEN (OCTINOXATE, OCTISALATE, ZINC OXIDE SUNSCREEN) LOTION [SWISS-AMERICAN CDMO, LLC]3Current NDC, Legacy NDC, 1 package rows20231109_f997f4fc-7da5-433c-9a53-2030b489b4f6.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
60232-0006-16023200060150 g in 1 BOTTLE (60232-0006-1) 50 g2011-08-310000-00-00NoNoCurrent