Home NDC 81352-321 SANTO REMEDIOS Piel Eterna Radiance Sunscreen Primer SPF-42
Product NDC 81352-321
11-digit product format 813520321
Labeler code 81352
Product ID 81352-321_09769ae3-d18d-e2dd-e063-6294a90a1f64
Type HUMAN OTC DRUG
Nonproprietary name TITANIUM DIOXIDE, ZINC OXIDE
Dosage form LOTION
Route TOPICAL
Labeler SANTO REMEDIO LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-03-21
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 60; 80 mg/mL; mg/mL
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 SANTO REMEDIOS Piel Eterna Radiance Sunscreen Primer SPF-42
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 60 mg/mL ZINC OXIDE 80 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP Internal UNII lookup SOI2LOH54Z 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 81352-321-00 SANTO REMEDIOS Piel Eterna Radiance Sunscreen Primer SPF-42 50 mL in 1 TUBE LOTION 50 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81352-321 SANTO REMEDIOS PIEL ETERNA RADIANCE SUNSCREEN PRIMER SPF-42 (TITANIUM DIOXIDE, ZINC OXIDE) LOTION [SANTO REMEDIO LLC] 2 Current NDC, Legacy NDC, 1 package rows 20231106_82d210bc-b7ca-4d74-be58-85f175a75058.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 81352-321-00 81352032100 50 mL in 1 TUBE (81352-321-00) 50 ml 2022-03-21 0000-00-00 No No Current