Home NDC 72014-201 HUSTLE BUTTER SPF 50 MINERAL SUNSCREEN
Product NDC 72014-201
11-digit product format 720140201
Labeler code 72014
Product ID 72014-201_5d2e9f33-d113-5bea-e063-6394a90a3181
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler H.B.D. DIST. INC.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-04-15
Substance ZINC OXIDE
Active strength 24 g/100mL
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 HUSTLE BUTTER SPF 50 MINERAL SUNSCREEN
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 24 g/100mL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72014-201-01 HUSTLE BUTTER SPF 50 MINERAL SUNSCREEN 88 mL in 1 TUBE LOTION 88 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72014-201 HUSTLE BUTTER SPF 50 MINERAL SUNSCREEN (ZINC OXIDE) LOTION [H.B.D. DIST. INC.] 1 Current NDC, 1 package rows 20250416_93e328b4-23dc-4484-aecb-5c41672bbf72.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 Units Marketing start Sample Exclude flag Status 72014-201-01 72014020101 88 mL in 1 TUBE (72014-201-01) 88 ml 2025-04-15 No No Current