Home NDC 71499-135 FENTY SKIN HYDRA VIZOR BROAD SPECTRUM MINERAL SPF 30 SUNSCREEN MOISTURIZER
Product NDC 71499-135
11-digit product format 714990135
Labeler code 71499
Product ID 71499-135_4008ee54-6804-cdcd-e063-6294a90a7a1d
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE
Dosage form CREAM
Route TOPICAL
Labeler KENDO HOLDINGS INC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-06-01
Substance ZINC OXIDE
Active strength 15.5 g/100mL
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 FENTY SKIN HYDRA VIZOR BROAD SPECTRUM MINERAL SPF 30 SUNSCREEN MOISTURIZER
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 15.5 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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71499-135-01 FENTY SKIN HYDRA VIZOR BROAD SPECTRUM MINERAL SPF 30 SUNSCREEN MOISTURIZER 50 mL in 1 TUBE CREAM 50 4 71499-135-01 FENTY SKIN HYDRA VIZOR BROAD SPECTRUM MINERAL SPF 30 SUNSCREEN MOISTURIZER 1 in 1 BOX CREAM 1 4 71499-135-02 FENTY SKIN HYDRA VIZOR BROAD SPECTRUM MINERAL SPF 30 SUNSCREEN MOISTURIZER 1 in 1 BOX CREAM 1 4 71499-135-02 FENTY SKIN HYDRA VIZOR BROAD SPECTRUM MINERAL SPF 30 SUNSCREEN MOISTURIZER 30 mL in 1 BOTTLE, PUMP CREAM 30 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71499-135 FENTY SKIN HYDRA VIZOR BROAD SPECTRUM MINERAL SPF 30 SUNSCREEN MOISTURIZER (ZINC OXIDE) CREAM [KENDO HOLDINGS INC] 3 Current NDC, 4 package rows 20240524_fd16def1-4c88-3ad0-e053-6294a90ab088.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 109 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 71499-135-01 71499013501 1 TUBE in 1 BOX (71499-135-01) / 50 mL in 1 TUBE 1 tube 2023-06-01 No No Current 71499-135-02 71499013502 1 BOTTLE, PUMP in 1 BOX (71499-135-02) / 30 mL in 1 BOTTLE, PUMP 2023-06-01 No No Current