Home NDC 87407-236 Knesko Skin The Sunscreen
Product NDC 87407-236
11-digit product format 874070236
Labeler code 87407
Product ID 87407-236_5114ef81-229c-690c-e063-6394a90a0cd0
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler Knesko, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-04-20
Substance ZINC OXIDE
Active strength 132 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 Knesko Skin The Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 132 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.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 87407-236-01 Knesko Skin The Sunscreen 50 mL in 1 BOTTLE LOTION 50 1 87407-236-02 Knesko Skin The Sunscreen 1 in 1 CARTON LOTION 1 1
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 87407-236-01 87407023601 50 mL in 1 BOTTLE 50 ml Historical 87407-236-02 87407023602 1 BOTTLE in 1 CARTON (87407-236-02) / 50 mL in 1 BOTTLE (87407-236-01) 1 bottle 2026-04-20 No No Current