Home NDC 87313-005 Hawaiian Blend Sensitive Zinc SPF 50
Product NDC 87313-005
11-digit product format 873130005
Labeler code 87313
Product ID 87313-005_47cfa4d4-cd8e-8d6d-e063-6394a90a6a4c
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide, Titanium Dioxide
Dosage form AEROSOL
Route TOPICAL
Labeler The Islander Group
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-01-03
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 4; 19.5 g/100g; g/100g
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 Hawaiian Blend Sensitive Zinc SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 4 g/100g ZINC OXIDE 19.5 g/100g
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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 87313-005-05 Hawaiian Blend Sensitive Zinc SPF 50 170 g in 1 CAN AEROSOL 170 2
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 87313-005-05 87313000505 170 g in 1 CAN (87313-005-05) 170 g 2023-01-03 No No Current