Home NDC 84723-006 Pipette Mineral Sunscreen SPF 50
Product NDC 84723-006
11-digit product format 847230006
Labeler code 84723
Product ID 84723-006_3b502e39-c815-30b3-e063-6394a90aa409
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE
Dosage form AEROSOL, SPRAY
Route TOPICAL
Labeler Pipette LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-08-01
Substance ZINC OXIDE
Active strength 20 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 Pipette Mineral Sunscreen SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 20 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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 84723-006-01 Pipette Mineral Sunscreen SPF 50 177 mL in 1 BOTTLE, SPRAY AEROSOL, SPRAY 177 2 84723-006-02 Pipette Mineral Sunscreen SPF 50 1 in 1 CARTON AEROSOL, SPRAY 1 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 162 of 353 · 7,049 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Status 84723-006-01 84723000601 177 mL in 1 BOTTLE, SPRAY 177 ml Historical 84723-006-02 84723000602 1 in 1 CARTON Historical