Home NDC 60232-0006 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 ZINC OXIDE; OCTINOXATE; OCTISALATE
Active strength 80; 75; 30 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 Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
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 Ingredient Strength ZINC OXIDE 80 g/1000g OCTINOXATE 75 g/1000g OCTISALATE 30 g/1000g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup 4Y5P7MUD51 Internal UNII lookup 4X49Y0596W Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 60232-0006-1 Private Label SPF45 Water Resistant Paraben Free Sunscreen 50 g in 1 BOTTLE LOTION 50 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 60232-0006 PRIVATE LABEL SPF45 WATER RESISTANT PARABEN FREE SUNSCREEN (OCTINOXATE, OCTISALATE, ZINC OXIDE SUNSCREEN) LOTION [SWISS-AMERICAN CDMO, LLC] 3 Current NDC, Legacy NDC, 1 package rows 20231109_f997f4fc-7da5-433c-9a53-2030b489b4f6.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 60232-0006-1 60232000601 50 g in 1 BOTTLE (60232-0006-1) 50 g 2011-08-31 0000-00-00 No No Current