Home NDC 60232-1830 Image Prevention Refiner Primer SPF50
Product NDC 60232-1830
11-digit product format 602321830
Labeler code 60232
Product ID 60232-1830_94652e72-a0f1-46f1-8698-89b8c39690f6
Type HUMAN OTC DRUG
Nonproprietary name Zinc oxide, titanium dioxide sunscreen
Dosage form CREAM
Route TOPICAL
Labeler Swiss-American CDMO, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-03-06
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 210; 50 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 Image Prevention Refiner Primer SPF50
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 210 g/1000g TITANIUM DIOXIDE 50 g/1000g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup 15FIX9V2JP Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 60232-1830-0 Image Prevention Refiner Primer SPF50 7 g in 1 TUBE CREAM 7 3 60232-1830-2 Image Prevention Refiner Primer SPF50 48 g in 1 TUBE CREAM 48 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 60232-1830 IMAGE PREVENTION REFINER PRIMER SPF50 (ZINC OXIDE, TITANIUM DIOXIDE SUNSCREEN) CREAM [SWISS-AMERICAN CDMO, LLC] 3 Current NDC, Legacy NDC, 2 package rows 20231108_0e490f11-666c-420c-8c12-b45cd238ce47.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 60232-1830-0 60232183000 7 g in 1 TUBE (60232-1830-0) 7 g 2020-03-09 0000-00-00 No No Current 60232-1830-2 60232183002 48 g in 1 TUBE (60232-1830-2) 48 g 2020-03-09 0000-00-00 No No Current