Home NDC 87618-101 Maniscreen Hydrating Mineral Hand Sunscreen SPF 25 Fragrance-Free
Product NDC 87618-101
11-digit product format 876180101
Labeler code 87618
Product ID 87618-101_5de7a929-b1b0-bbba-e063-6294a90a00ab
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler Underlining, Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-14
Substance ZINC OXIDE
Active strength 357 mg/mL
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 Maniscreen Hydrating Mineral Hand Sunscreen SPF 25 Fragrance-Free
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 357 mg/mL
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.
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 Marketing start Sample Exclude flag Status 87618-101-01 87618010101 1 BOTTLE, PUMP in 1 CARTON (87618-101-01) / 30 mL in 1 BOTTLE, PUMP 2026-08-14 No No Current