Home NDC 85966-002 Pure6 ManiShield Hand Screen
Product NDC 85966-002
11-digit product format 859660002
Labeler code 85966
Product ID 85966-002_3dcede54-b5fa-cab2-e063-6294a90aab08
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE, TITANIUM DIOXIDE
Dosage form LIQUID
Route TOPICAL
Labeler GUANGZHOU SAWEILAN IMPORT & EXPORT TRADING CO., LTD
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-07-25
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 10; 2.5 g/50g; g/50g
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 Pure6 ManiShield Hand Screen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 10 g/50g TITANIUM DIOXIDE 2.5 g/50g
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.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85966-002-01 Pure6 ManiShield Hand Screen 50 g in 1 BOTTLE LIQUID 50 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 85966-002-01 85966000201 50 g in 1 BOTTLE (85966-002-01) 50 g 2025-07-25 No No Current