Home NDC 73251-010 Purito Sunday Adventure Sunscreen SPF 50, 50 mL
Product NDC 73251-010
11-digit product format 732510010
Labeler code 73251
Product ID 73251-010_4e5656c1-3867-9f19-e063-6394a90ab7c8
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form CREAM
Route TOPICAL
Labeler Hinature
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-02-15
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength 30; 90; 45; 50 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
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 Purito Sunday Adventure Sunscreen SPF 50, 50 mL
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/mL HOMOSALATE 90 mg/mL OCTISALATE 45 mg/mL OCTOCRYLENE 50 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 73251-010-00 Purito Sunday Adventure Sunscreen SPF 50, 50 mL 50 mL in 1 BOTTLE CREAM 50 7 73251-010-01 Purito Sunday Adventure Sunscreen SPF 50, 50 mL 50 mL in 1 TUBE CREAM 50 7 73251-010-02 Purito Sunday Adventure Sunscreen SPF 50, 50 mL 1 in 1 PACKAGE CREAM 1 7 73251-010-02 Purito Sunday Adventure Sunscreen SPF 50, 50 mL 60 mL in 1 TUBE CREAM 60 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73251-010 PURITO SUNDAY ADVENTURE SUNSCREEN SPF 50, 50 ML (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) CREAM [HINATURE] 5 Current NDC, 4 package rows 20250216_bf16f535-97fc-4fd8-9310-8b6bbc82baae.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 Sample Exclude flag Status 73251-010-00 73251001000 50 mL in 1 BOTTLE 50 ml Historical 73251-010-01 73251001001 50 mL in 1 TUBE (73251-010-01) 50 ml 2025-02-15 No No Current 73251-010-02 73251001002 1 TUBE in 1 PACKAGE (73251-010-02) / 60 mL in 1 TUBE 1 tube 2026-04-01 No No Current