Home NDC 70484-008 SPF 50 Daily UV Defense Broad Spectrum Sunscreen
Product NDC 70484-008
11-digit product format 704840008
Labeler code 70484
Product ID 70484-008_37f244fd-c02e-e66a-e063-6394a90aed81
Type HUMAN OTC DRUG
Nonproprietary name Octinoxate, Zinc Oxide
Dosage form CREAM
Route TOPICAL
Labeler Vi Medical Products, INC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-02-06
Substance ZINC OXIDE; OCTINOXATE
Active strength 10.8; 7.5 g/100mL; g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 70484-008 70484-008-04 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 70484-008 70484-008-04 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
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 SPF 50 Daily UV Defense Broad Spectrum Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 10.8 g/100mL OCTINOXATE 7.5 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup 4Y5P7MUD51 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 70484-008-01 SPF 50 Daily UV Defense Broad Spectrum Sunscreen 59 mL in 1 TUBE CREAM 59 3 70484-008-02 SPF 50 Daily UV Defense Broad Spectrum Sunscreen 1 in 1 CARTON CREAM 1 3 70484-008-03 SPF 50 Daily UV Defense Broad Spectrum Sunscreen 30 mL in 1 TUBE CREAM 30 3 70484-008-04 SPF 50 Daily UV Defense Broad Spectrum Sunscreen 1 in 1 CARTON CREAM 1 3 70484-008-05 SPF 50 Daily UV Defense Broad Spectrum Sunscreen 22 mL in 1 TUBE CREAM 22 3 70484-008-06 SPF 50 Daily UV Defense Broad Spectrum Sunscreen 1 in 1 BOX CREAM 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70484-008 SPF 50 DAILY UV DEFENSE BROAD SPECTRUM SUNSCREEN (OCTINOXATE, ZINC OXIDE) CREAM [VI MEDICAL PRODUCTS, INC] 2 Current NDC, 6 package rows 20250223_2d814f8a-23b5-209f-e063-6394a90a5091.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 70484-008-01 70484000801 59 mL in 1 TUBE 59 ml Historical 70484-008-02 70484000802 1 TUBE in 1 CARTON (70484-008-02) / 59 mL in 1 TUBE (70484-008-01) 1 tube 2025-02-06 No No Current 70484-008-03 70484000803 30 mL in 1 TUBE 30 ml Historical 70484-008-04 70484000804 1 in 1 CARTON Historical 70484-008-05 70484000805 22 mL in 1 TUBE 22 ml Historical 70484-008-06 70484000806 1 TUBE in 1 BOX (70484-008-06) / 22 mL in 1 TUBE (70484-008-05) 1 tube 2025-08-15 No No Current