Home DailyMed 14d80223-b1c2-4f85-b0bd-7b7e4d5b5c5d High Protection Sun Air Spray SPF50 PA Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer The Doctor's Cosmetic Inc
Effective date 2009-10-01
Label type HUMAN OTC DRUG LABEL
Version 3
Source full-release
Hydrated at 2026-05-31 22:22:53 Label at a glance# Product High Protection Sun Air Spray SPF50 PA
Active ingredient OCTINOXATE
Label structure 4 sections
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43948-6001-1 High Protection Sun Air Spray SPF50 PA 130 mL in 1 BOTTLE, SPRAY SPRAY 130 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43948-6001 HIGH PROTECTION SUN AIR SPRAY SPF50 PA (OCTINOXATE OCTISALATE ALUMINUM HYDROXIDE) SPRAY [THE DOCTOR'S COSMETIC INC] 3 Legacy NDC, 1 package rows 20091208_14d80223-b1c2-4f85-b0bd-7b7e4d5b5c5d.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII SPL version Uploaded OCTINOXATE ACTIVE INGREDIENT 4Y5P7MUD51 3 OCTINOXATE ACTIVE MOIETY 4Y5P7MUD51 3 ALUMINUM HYDROXIDE INACTIVE INGREDIENT 5QB0T2IUN0 3 OCTISALATE INACTIVE INGREDIENT 4X49Y0596W 3
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 5 matching rows.
High Protection Sun Air Spray SPF50 PA OCTINOXATE OCTISALATE ALUMINUM HYDROXIDE OCTISALATE ALUMINUM HYDROXIDE OCTINOXATE Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 3 matching rows.
Inactive ingredient matches# Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
Inactive ingredient links page 1 of 1 · 7 matching rows.
DailyMed ingredient, IID ingredient, UNII table DailyMed ingredient IID ingredient UNII Dosage form / route Potency Maximum daily exposure Match ALUMINUM HYDROXIDE ALUMINUM HYDROXIDE 5QB0T2IUN0 CREAM / TOPICAL 5 %w/w Exact identifier — unii candidate 4 equally ranked IID candidates OCTISALATE OCTISALATE 4X49Y0596W SOLUTION / TOPICAL 300 mg Exact identifier — unii candidate 3 equally ranked IID candidates ALUMINUM HYDROXIDE ALUMINUM HYDROXIDE 5QB0T2IUN0 OINTMENT / TOPICAL NA Exact identifier — unii candidate 4 equally ranked IID candidates OCTISALATE OCTISALATE 4X49Y0596W SOLUTION / TRANSDERMAL 5 %w/v Exact identifier — unii candidate 3 equally ranked IID candidates ALUMINUM HYDROXIDE ALUMINUM HYDROXIDE 5QB0T2IUN0 TABLET / ORAL 50 mg Exact identifier — unii candidate 4 equally ranked IID candidates ALUMINUM HYDROXIDE ALUMINUM HYDROXIDE 5QB0T2IUN0 CAPSULE / ORAL NA Exact identifier — unii candidate 4 equally ranked IID candidates OCTISALATE OCTISALATE 4X49Y0596W SPRAY / TRANSDERMAL 8.5 %w/v Exact identifier — unii candidate 3 equally ranked IID candidates
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 1 of 1 · 1 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
