Home NDC 61973-100 Arizona Sun Sunscreen SPF 8
Product NDC 61973-100
11-digit product format 619730100
Labeler code 61973
Product ID 61973-100_4f0c8f3f-68e2-8c30-e063-6394a90a6805
Type HUMAN OTC DRUG
Nonproprietary name Sunscreen
Dosage form LOTION
Route TOPICAL
Labeler Arizona Sun Products
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-02-02
Substance OCTISALATE; OXYBENZONE; OCTINOXATE
Active strength 10; 10; 65 mg/g; mg/g; mg/g
NDC exclude flag No
Listing certified through 2027-12-31
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 · 24 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 61973-100-04 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 61973-100-04 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 61973-100-04 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 61973-100-04 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 61973-100-04 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 61973-100-04 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 61973-100-04 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 61973-100-04 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 61973-100-04 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 61973-100-04 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 61973-100-04 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 61973-100-04 557ba5c1ecfa…9c80585c8c6e…
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 Arizona Sun Sunscreen SPF 8
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 10 mg/g OXYBENZONE 10 mg/g OCTINOXATE 65 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4X49Y0596W Internal UNII lookup 95OOS7VE0Y Internal UNII lookup 4Y5P7MUD51 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 61973-100-04 Arizona Sun Sunscreen SPF 8 120 g in 1 BOTTLE LOTION 120 4
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 113 of 354 · 7,077 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join UV Defense Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE CCLEAR SOLUTIONS ACNE & SKIN CARE CLINIC 365e09a8-308b-b753-e063-6394a90ae9e5 2025-12-16 Exact identifier application number: M020 UV Defense Mineral Sunscreen Tinted TITANIUM DIOXIDE, ZINC OXIDE CCLEAR SOLUTIONS ACNE & SKIN CARE CLINIC 365e2498-7df2-f22c-e063-6294a90ac6ab 2025-12-16 Exact identifier application number: M020 UV Protection Veil Mineral Sunscreen non tinted TITANIUM DIOXIDE, ZINC OXIDE ATHENA PLASTIC SURGERY 3b3bf5a6-33ec-0255-e063-6294a90ac96a 2025-12-16 Warnings Exact identifier application number: M020 UV Protection Veil Mineral Sunscreen, tinted TITANIUM DIOXIDE, ZINC OXIDE ATHENA PLASTIC SURGERY 3b3cba2e-acc6-a2df-e063-6294a90abf71 2025-12-16 Warnings Exact identifier application number: M020 Color Smart Tinted Mineral ZINC OXIDE MEGAN YORK INC. 365c4623-94d5-e8b6-e063-6394a90a966a 2025-12-16 Exact identifier application number: M020 Anti-Aging Tinted Sunscreen ZINC OXIDE KARINA SALDIVAR 3bca508e-7bd0-d45d-e063-6394a90a1730 2025-12-16 Warnings Exact identifier application number: M020 UV Protection Veil Mineral Sunscreen, tinted TITANIUM DIOXIDE, ZINC OXIDE ATHENA PLASTIC SURGERY 3b3c757f-6581-4978-e063-6294a90a6173 2025-12-16 Warnings Exact identifier application number: M020 Kind Restore Tinted Mineral Sunscreen ZINC OXIDE POLISH BEAUTY 3980810f-58b5-3a60-e063-6294a90a9c07 2025-12-16 Exact identifier application number: M020 Daydream Beyond Screen ZINC OXIDE ULTRAVIOLET SKINCARE LLC 36bfd963-d123-0d25-e063-6294a90aa827 2025-12-16 Exact identifier application number: M020 Virgo SOL Primer Sunscreen TITANIUM DIOXIDE, ZINC OXIDE ULTRAVIOLET SKINCARE LLC 369d4f43-8c57-9fcf-e063-6294a90aa916 2025-12-16 Exact identifier application number: M020 Virgo SOL Non Tinted Mousse TITANIUM DIOXIDE, ZINC OXIDE ULTRAVIOLET SKINCARE LLC 369d63a9-b9ab-9530-e063-6394a90ac8ef 2025-12-16 Exact identifier application number: M020 Kind Restore Tinted Mineral Sunscreen ZINC OXIDE POLISH BEAUTY 3980d278-c0f4-2c59-e063-6394a90aac37 2025-12-16 Exact identifier application number: M020 Solar Eclipse Extreme Sunscreen ZINC OXIDE ULTRAVIOLET SKINCARE LLC 36bfa691-48c0-8033-e063-6294a90ad899 2025-12-16 Exact identifier application number: M020 Kind Restore Moisturizing Lip Balm TITANIUM DIOXIDE, ZINC OXIDE POLISH BEAUTY 39814e27-4f3f-5ee6-e063-6394a90a941b 2025-12-16 Exact identifier application number: M020 Yoali SPF 40 ZINC OXIDE YOALI STUDIO LLC 390b7f9c-bc04-80ec-e063-6294a90a4092 2025-12-16 Exact identifier application number: M020 Skin Defense Matte Tinted Sunscreen ZINC OXIDE Gentlehomme LLC 365eb727-3e7f-f1dd-e063-6394a90aa469 2025-12-16 Exact identifier application number: M020 Dr B Clinical Skin Care Tinted Sunscreen TITANIUM DIOXIDE, ZINC OXIDE NAIRA BABAIAN, M.D., P.A. 365da1f8-5250-7589-e063-6294a90a3e68 2025-12-16 Exact identifier application number: M020 Dr B Clinical Skin Care Non Tinted Sunscreen TITANIUM DIOXIDE, ZINC OXIDE NAIRA BABAIAN, M.D., P.A. 365d7564-3025-257b-e063-6294a90ad170 2025-12-16 Exact identifier application number: M020 Tinted Mineral Sunscreen ZINC OXIDE Gentlehomme LLC 365e7d8e-e3e0-4c08-e063-6294a90af415 2025-12-16 Exact identifier application number: M020 Daily Replenish mineral sunscreen ZINC OXIDE PURE VITALITY SKIN AND BODY, INC 369896b1-f4b4-6201-e063-6394a90a5bca 2025-12-16 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 61973-100-04 61973010004 120 g in 1 BOTTLE (61973-100-04) 120 g 2024-02-02 No No Current