Home NDC 70484-005 Sunscreen Broad Spectrum SPF 50
Product NDC 70484-005
11-digit product format 704840005
Labeler code 70484
Product ID 70484-005_2e225a04-5b1a-899c-e063-6294a90a127f
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide, Octinoxate
Dosage form CREAM
Route TOPICAL
Labeler Vi Medical Products, INC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-03-26
Substance ZINC OXIDE; OCTINOXATE
Active strength 10; 7.5 g/100mL; g/100mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
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 · 39 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-02-02 03:52 UTC · source 2025-01-31 excluded product product I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 70484-005-02 I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 70484-005-04 I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 70484-005-02 I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 70484-005-04 I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 70484-005-02 I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 70484-005-04 I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 70484-005-02 I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 70484-005-04 I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 70484-005-02 I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 70484-005-04 I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 70484-005-02 I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 70484-005-04 I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 70484-005-02 I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 70484-005-04 I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product I Inactivated by FDA 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 70484-005-02 I Inactivated by FDA 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 70484-005-04 I Inactivated by FDA 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 70484-005-02 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 70484-005-04 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 70484-005-04 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 70484-005-02 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 70484-005-04 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 70484-005-02 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 70484-005-04 I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 70484-005-02 I Inactivated by FDA bd6a592717d7…303034d00443…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 70484-005-04 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 70484-005-02 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
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 Sunscreen Broad Spectrum SPF 50
Brand name suffix Vi Aesthetics
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 10 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# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70484-005-01 Sunscreen Broad Spectrum SPF 50Vi Aesthetics 30 mL in 1 TUBE CREAM 30 6 70484-005-02 Sunscreen Broad Spectrum SPF 50Vi Aesthetics 1 in 1 BOX CREAM 1 6 70484-005-03 Sunscreen Broad Spectrum SPF 50Vi Aesthetics 59 mL in 1 TUBE CREAM 59 6 70484-005-04 Sunscreen Broad Spectrum SPF 50Vi Aesthetics 1 in 1 BOX CREAM 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70484-005 SUNSCREEN BROAD SPECTRUM SPF 50 VI AESTHETICS (ZINC OXIDE, OCTINOXATE) CREAM [VI MEDICAL PRODUCTS, INC] 6 Current NDC, Legacy NDC, 4 package rows 20250216_73620765-c7c0-4bd7-82a9-00022773c928.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 286 of 346 · 6,912 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Bright as Day Mineral SPF50 ZINC OXIDE Koco Life LLC 1c245a53-4098-62e6-e063-6294a90abf12 2024-09-23 Warnings Exact identifier application number: M020 Pure Protect Mineral Sunscreen Stick SPF50 ZINC OXIDE Koco Life LLC 22cd5999-9b9a-91a3-e063-6394a90a0da5 2024-09-23 Warnings Exact identifier application number: M020 ABSOLUTELY natural Lip Balm Broad Spectrum SPF 15 Sunscreen ZINC OXIDE Absolutely Natural eb914dd8-9b11-44dd-8c4f-4d4c0c3bf1ea 2024-09-23 Warnings Exact identifier application number: M020 SUNSCREEN 01 AVOBENZONE,HOMOSALATE,OCTOCRYLENE,OCTISALATE Cosmuses Cosmetics (Ningbo) Co., Ltd. 229dabbc-9043-3c9d-e063-6394a90a5692 2024-09-21 Warnings Exact identifier application number: M020 GLC OG Natural Tinted SPF 30 Sunscreen ZINC OXIDE GUD LIFE CO. LLC 25e1e8ec-e19d-45f7-b339-5d12c2b511d6 2024-09-18 Warnings Exact identifier application number: M020 Target Up and Up Sunscreen SPF 30 SPORT Broad Spectrum AVOBENZONE, HOMOSALATE,OCTISALATE,OCTOCRYLENE TARGET CORPORATION bad7d56e-662e-0776-e053-2a95a90a0af0 2024-09-18 Warnings Exact identifier application number: M020 Target Up and Up Kids SPF 50 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE TARGET CORPORATION b82b6d0d-616d-f041-e053-2995a90ae6a3 2024-09-18 Warnings Exact identifier application number: M020 COOLA Dew Good Illuminating Body Melt SPF 40 AVOBENZONE, OCTISALATE, OCTOCRYLENE COOLA LLC 43d293f6-e13c-4ee9-89df-2a3ef0034e31 2024-09-16 Warnings Exact identifier application number: M020 Proceuticals Private Label by TiZO non-tinted replenishing daily protection ZINC OXIDE Fallien Cosmeceuticals, Ltd 2203ea22-d12a-99fe-e063-6394a90aca9f 2024-09-13 Warnings Exact identifier application number: M020 OS-01 Face SPF BS SPF30 Tinted ZINC OXIDE Allure Labs 22042031-ac8e-1ab2-e063-6394a90a6ed4 2024-09-13 Warnings Exact identifier application number: M020 OS-01 Face SPF BS SPF30 Tinted ZINC OXIDE ONESKIN INC. 2204e776-b1a1-be15-e063-6294a90af5de 2024-09-13 Warnings Exact identifier application number: M020 OS-01 Face SPF BS SPF30 Untinted ZINC OXIDE Allure Labs 2205345b-5e92-37eb-e063-6294a90a6b6c 2024-09-13 Warnings Exact identifier application number: M020 OS-01 Face SPF BS SPF30 Untinted ZINC OXIDE ONESKIN INC. 2205ec0e-ac3f-299f-e063-6294a90a2174 2024-09-13 Warnings Exact identifier application number: M020 H-E-B SOLUTIONS SUNSCREEN COCONUT SPF 50 CONTINUOUS AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE H.E.B f4130277-ea9b-6b25-e053-2a95a90a59be 2024-09-13 Warnings Exact identifier application number: M020 HEB SPF 50 Tattoo Continuous Sunscreen AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE H.E.B f6df491d-1fa9-a4c8-e053-6394a90a3866 2024-09-13 Warnings Exact identifier application number: M020 YOUR Day Cream Sunscreen Broad Spectrum SPF 30 OCTISALATE, OXYBENZONE, AVOBENZONE, OCTOCRYLENE Skin Ai, LLC 21cbd5ac-5307-939b-e063-6294a90ac791 2024-09-10 Warnings Exact identifier application number: M020 Mario Badescu SPF 17 AVOBENZONE, OCTINOXATE, OCTOCRYLENE Bentley Laboratories LLC 0fd51f8d-ee67-48fd-ab98-1fedb0339462 2024-09-10 Warnings Exact identifier application number: M020 Mario Badescu Collagen SPF 15 AVOBENZONE, OCTINOXATE, OXYBENZONE Bentley Laboratories LLC 0246b11b-f1ba-4f47-91ab-52a6554b9467 2024-09-10 Warnings Exact identifier application number: M020 Mario Badescu The Moisture Magnet SPF 15 AVOBENZONE, OCTINOXATE, OXYBENZONE Bentley Laboratories LLC f6d653f5-52a0-42ad-8308-b8d6f57050cc 2024-09-10 Warnings Exact identifier application number: M020 MARIO BADESCU SPF 30 AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE Bentley Laboratories LLC fe485d4c-0ded-4061-ac34-77b72d535090 2024-09-10 Warnings Exact identifier application number: M020
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70484-005-01 70484000501 30 mL in 1 TUBE 30 ml Historical 70484-005-02 70484000502 1 TUBE in 1 BOX (70484-005-02) / 30 mL in 1 TUBE (70484-005-01) 1 tube 2015-03-26 0000-00-00 No No Current 70484-005-03 70484000503 59 mL in 1 TUBE 59 ml Historical 70484-005-04 70484000504 1 TUBE in 1 BOX (70484-005-04) / 59 mL in 1 TUBE (70484-005-03) 1 tube 2015-03-26 0000-00-00 No No Current