Home NDC 81568-101 dr. brandt SUN SHIELD SPF 50
Product NDC 81568-101
11-digit product format 815680101
Labeler code 81568
Product ID 81568-101_d6922659-fdc4-48c0-a7d6-a3051be051c1
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form LIQUID
Route TOPICAL
Labeler Dr. Brandt
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-02-15
Substance ZINC OXIDE
Active strength 17 g/100mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
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 dr. brandt SUN SHIELD SPF 50
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 17 g/100mL
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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81568-101-50 dr. brandt SUN SHIELD SPF 50 50 mL in 1 BOTTLE, DROPPER LIQUID 50 2 81568-101-50 dr. brandt SUN SHIELD SPF 50 1 in 1 BOX LIQUID 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81568-101 DR. BRANDT SUN SHIELD SPF 50 (ZINC OXIDE) LIQUID [DR. BRANDT] 2 Current NDC, Legacy NDC, 2 package rows 20240907_6f8af59b-d423-4250-8ddc-061fea886e3e.zip
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 Marketing start Marketing end Sample Exclude flag Status 81568-101-50 81568010150 1 BOTTLE, DROPPER in 1 BOX (81568-101-50) / 50 mL in 1 BOTTLE, DROPPER 2021-02-15 0000-00-00 No No Current