Home NDC 58466-109 78 x 36 SPF 30 Active
Product NDC 58466-109
11-digit product format 584660109
Labeler code 58466
Product ID 58466-109_1c2b73fd-1c52-4db3-982e-d937c04ceeac
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE
Dosage form CREAM
Route TOPICAL
Labeler Dermazone LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-10-01
Substance ZINC OXIDE
Active strength .2 g/g
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 · 14 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 2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 58466-109-03 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 58466-109-03 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 58466-109-03 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 58466-109-03 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 58466-109-03 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 58466-109-03 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 58466-109-03 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
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 78 x 36 SPF 30 Active
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE .2 g/g
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 Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 58466-109-03 78 x 36 SPF 30 Active 96 g in 1 TUBE CREAM 96 2 58466-109-03 78 x 36 SPF 30 Active 1 in 1 CARTON CREAM 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58466-109 78 X 36 SPF 30 ACTIVE (ZINC OXIDE) CREAM [DERMAZONE SOLUTIONS, INC.] 1 Current NDC, 2 package rows 20231001_96a8aacc-5c2f-410a-8fb4-8b3bc0f81e55.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 134 of 353 · 7,041 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Tinted Primer Anti-Aging TITANIUM DIOXIDE, ZINC OXIDE DERMOPERFECTION SKINCARE SERVICES, LLC 351aaaad-44ce-3558-e063-6294a90a2b46 2025-12-11 Exact identifier application number: M020 Total Body Block Sunscreen ZINC OXIDE ADR SUNCARE 38f4928c-6389-5aa1-e063-6294a90a8f9d 2025-12-11 Exact identifier application number: M020 Magic Veil ZINC OXIDE THE COMPLEXIONIST 38f574ad-c4bf-fca1-e063-6394a90a00c5 2025-12-11 Exact identifier application number: M020 Magic Veil ZINC OXIDE THE COMPLEXIONIST 38f5a0b9-bbe2-50f4-e063-6294a90a10d7 2025-12-11 Exact identifier application number: M020 Daily Tinted Antioxidant Mineral Sunscreen ZINC OXIDE MONIKA G KIRIPOLSKY MD INC. 3b3f19c1-4bff-315f-e063-6394a90a9a85 2025-12-11 Warnings Exact identifier application number: M020 Daily Repair Moisturizing Tinted ZINC OXIDE Skintique 37dd83db-aa43-7f66-e063-6294a90a893b 2025-12-11 Exact identifier application number: M020 Daily Repair Moisturizing Non Tinted ZINC OXIDE Skintique 37de01d0-7694-69c1-e063-6394a90acf0a 2025-12-11 Exact identifier application number: M020 Daily Shield Facial Primer TITANIUM DIOXIDE, ZINC OXIDE Skintique 37dd5228-5fe4-5e7b-e063-6294a90adffb 2025-12-11 Exact identifier application number: M020 Daily Repair Moisturizing Non Tinted ZINC OXIDE Skintique 37ddc177-376d-b2fe-e063-6294a90a5e07 2025-12-11 Exact identifier application number: M020 Daily Shield Facial Primer TITANIUM DIOXIDE, ZINC OXIDE Skintique 37de2f44-e0da-0d1c-e063-6294a90ae18b 2025-12-11 Exact identifier application number: M020 Daily Repair Moisturizing Tinted ZINC OXIDE Skintique 37de5a51-0bc4-34ad-e063-6294a90a0eef 2025-12-11 Exact identifier application number: M020 Mineral Sunscreen ZINC OXIDE LEILANI VIDAL 36d51157-1bcd-79c8-e063-6394a90aba71 2025-12-11 Exact identifier application number: M020 Mineral Sunscreen ZINC OXIDE LEILANI VIDAL 36d4b998-c29c-ff89-e063-6394a90a12d8 2025-12-11 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE LEILANI VIDAL 36d5831a-7128-729a-e063-6394a90a8036 2025-12-11 Exact identifier application number: M020 Mineral Matte Non-Tinted Sunscreen TITANIUM DIOXIDE, ZINC OXIDE ORAIOS BEAUTY LLC 3ac219bd-dfc8-fe22-e063-6394a90a4a8c 2025-12-11 Warnings Exact identifier application number: M020 Tinted Facial Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE ORAIOS BEAUTY LLC 3ac25d06-d885-48a2-e063-6294a90a0d0b 2025-12-11 Warnings Exact identifier application number: M020 Tinted Mineral Lip Sunscreen TITANIUM DIOXIDE, ZINC OXIDE ORAIOS BEAUTY LLC 3ac27b6c-1341-1f05-e063-6394a90a9860 2025-12-11 Warnings Exact identifier application number: M020 Facial Mineral Sunscreen Tinted TITANIUM DIOXIDE, ZINC OXIDE DR. CARIN GRIBETZ BOARD CERTIFIED DERMATOLOGIST 37287e4c-6fdf-62c5-e063-6394a90a1296 2025-12-11 Exact identifier application number: M020 Facial Mineral Sunscreen Non Tinted TITANIUM DIOXIDE, ZINC OXIDE DR. CARIN GRIBETZ BOARD CERTIFIED DERMATOLOGIST 37284de3-32d4-3611-e063-6394a90a6393 2025-12-11 Exact identifier application number: M020 Mineral Lip Sunscreen Tinted TITANIUM DIOXIDE, ZINC OXIDE DR. CARIN GRIBETZ BOARD CERTIFIED DERMATOLOGIST 3728ec6a-7de5-bbc5-e063-6294a90a31b7 2025-12-11 Exact identifier application number: M020
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 58466-109-03 58466010903 1 TUBE in 1 CARTON (58466-109-03) / 96 g in 1 TUBE 1 tube 2023-10-01 No No Current