Home NDC 73418-108 Zinc Oxide Titanium Oxide
Product NDC 73418-108
11-digit product format 734180108
Labeler code 73418
Product ID 73418-108_3e7753f0-4ef8-e165-e063-6294a90a11db
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide Titanium Oxide
Dosage form LOTION
Route TOPICAL
Labeler Hello Bello
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-05-09
Substance ZINC OXIDE
Active strength 23 mg/g
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 Zinc Oxide Titanium Oxide
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 23 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 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 73418-108-01 Zinc Oxide Titanium Oxide 141.748 g in 1 TUBE LOTION 141.748 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 238 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 73418-108-01 73418010801 141.748 g in 1 TUBE (73418-108-01) 141.748 g 2025-09-09 No No Current