Home NDC 73418-111 Kids Mineral Sunscreen SPF 50
Product NDC 73418-111
11-digit product format 734180111
Labeler code 73418
Product ID 73418-111_5b19f2bc-0df5-c427-e063-6394a90a0a45
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form SPRAY
Route TOPICAL
Labeler Hello Bello
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-09-09
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 22.25; 4.82 mg/g; mg/g
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 Kids Mineral Sunscreen SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 22.25 mg/g TITANIUM DIOXIDE 4.82 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup 15FIX9V2JP Internal UNII lookup
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 302 of 346 · 6,912 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 73418-111-01 73418011101 142 g in 1 BOTTLE, SPRAY (73418-111-01) 142 g 2026-09-09 No No Current