Home NDC 87838-002 Aussie Betta Tallow Sunscreen SPF50
Product NDC 87838-002
11-digit product format 878380002
Labeler code 87838
Product ID 87838-002_56048d71-fa3d-48cd-e063-6394a90a33e5
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide and Zinc Oxide Sunscreen
Dosage form CREAM
Route TOPICAL
Labeler AUSSIE BETTA HEALTHY CARE PTY LTD
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-07
Substance ZINC OXIDE; TITANIUM DIOXIDE; ETHYLHEXYL SALICYLATE; OCTOCRYLENE
Active strength 13; 6.4; 4; 6 g/100g; g/100g; 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 Aussie Betta Tallow Sunscreen SPF50
Brand name suffix SPF50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 13 g/100g TITANIUM DIOXIDE 6.4 g/100g ETHYLHEXYL SALICYLATE 4 g/100g OCTOCRYLENE 6 g/100g
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.
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 87838-002-01 87838000201 50 g in 1 TUBE (87838-002-01) 50 g 2026-07-07 No No Current 87838-002-02 87838000202 80 g in 1 TUBE (87838-002-02) 80 g 2026-07-07 No No Current