Home NDC 70412-817 SPF30 Sunscreen and Antibacterial Hand Sanitizer
Product NDC 70412-817
11-digit product format 704120817
Labeler code 70412
Product ID 70412-817_09874009-51eb-ac30-e063-6394a90ae5b4
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL, AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE
Dosage form KIT
Route TOPICAL
Labeler Zhejiang Ayan Biotech Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-09-01
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 SPF30 Sunscreen and Antibacterial Hand Sanitizer
Listing expiration 2026-12-31 Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1020364 Internal RxNorm 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 70412-119-05 SPF30 Sunscreen and Antibacterial Hand Sanitizer 5 mL in 1 BOTTLE SPRAY 5 mL 620 mg in 1mL 6 70412-119-05 SPF30 Sunscreen and Antibacterial Hand Sanitizer 1 in 1 BOX SPRAY 620 mg in 1mL 6 70412-238-05 SPF30 Sunscreen and Antibacterial Hand Sanitizer 5 mL in 1 TUBE SPRAY 5 mL 50 mg in 1mL 6 70412-817-05 SPF30 Sunscreen and Antibacterial Hand Sanitizer 1 in 1 KIT KIT 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70412-817 SPF30 SUNSCREEN AND ANTIBACTERIAL HAND SANITIZER (ALCOHOL, AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE) KIT [ZHEJIANG AYAN BIOTECH CO., LTD.] 6 Current NDC, Legacy NDC, 4 package rows 20231108_b5e2458f-8e84-4e57-b6f7-e428a94c97a4.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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70412-119-05 70412011905 5 mL in 1 BOTTLE 5 ml Historical 70412-238-05 70412023805 5 mL in 1 TUBE 5 ml Historical 70412-817-05 70412081705 1 KIT in 1 KIT (70412-817-05) * 1 BOTTLE in 1 BOX (70412-119-05) / 5 mL in 1 BOTTLE * 5 mL in 1 TUBE (70412-238-05) 1 kit 2018-09-01 0000-00-00 No No Current