Home NDC 71499-220 FENTY SKIN HYDRA VIZOR
Product NDC 71499-220
11-digit product format 714990220
Labeler code 71499
Product ID 71499-220_4008ebc9-50c8-80d7-e063-6394a90af954
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTISALATE
Dosage form LOTION
Route TOPICAL
Labeler KENDO HOLDINGS INC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-08-23
Substance AVOBENZONE; HOMOSALATE; OCTISALATE
Active strength 3; 9; 4.5 g/100mL; g/100mL; 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
Brand name suffix SPF 30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 3 g/100mL HOMOSALATE 9 g/100mL OCTISALATE 4.5 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G63QQF2NOX Internal UNII lookup V06SV4M95S Internal UNII lookup 4X49Y0596W 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 71499-220-01 FENTY SKIN HYDRA VIZORSPF 30 7 mL in 1 TUBE LOTION 7 7 71499-220-02 FENTY SKIN HYDRA VIZORSPF 30 30 mL in 1 TUBE LOTION 30 7 71499-220-03 FENTY SKIN HYDRA VIZORSPF 30 50 mL in 1 BOTTLE LOTION 50 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71499-220 FENTY SKIN HYDRA VIZOR SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE) LOTION [KENDO HOLDINGS INC] 6 Current NDC, Legacy NDC, 3 package rows 20240108_1d26bfb0-3c05-4a0c-9d4b-810359222730.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 Marketing end Sample Exclude flag Status 71499-220-01 71499022001 7 mL in 1 TUBE (71499-220-01) 7 ml 2020-08-23 0000-00-00 No No Current 71499-220-02 71499022002 30 mL in 1 TUBE (71499-220-02) 30 ml 2020-08-23 0000-00-00 No No Current 71499-220-03 71499022003 50 mL in 1 BOTTLE (71499-220-03) 50 ml 2020-08-23 0000-00-00 No No Current