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 163 of 353 · 7,049 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Sunsolve MD Volumize and Condition Lip ZINC OXIDE Sunsolve MD 396b7462-d597-4bf7-e063-6394a90ab58d 2025-11-14 Warnings Exact identifier application number: M020 Sunsovle MD Volumize and Restore ZINC OXIDE Sunsolve MD Inc 26f3cdda-b990-15cb-e063-6394a90ade29 2025-11-14 Warnings Exact identifier application number: M020 Naturium Dew-Glow Moisturizer SPF 50 HOMOSALATE, OCTISALATE, AVOBENZONE e.l.f. Cosmetics, Inc 0a5b80fb-caeb-eb56-e063-6294a90a238b 2025-11-14 Warnings Exact identifier application number: M020 Naturium Dew Glow Tinted Moisturizer SPF50 HOMOSALATE, OCTISALATE, AVOBENZONE e.l.f. Cosmetics, Inc. 0d82f310-f87a-f76d-e063-6294a90af251 2025-11-14 Warnings Exact identifier application number: M020 Naturium Dew Glow Tinted Moisturizer SPF50-deep HOMOSALATE, OCTISALATE, AVOBENZONE e.l.f. Cosmetics, Inc. 0d865e74-1baf-6a44-e063-6394a90a37ac 2025-11-14 Warnings Exact identifier application number: M020 Naturium Dew Glow Tinted Moisturizer SPF50-medium HOMOSALATE, OCTISALATE, AVOBENZONE e.l.f. Cosmetics, Inc. 0d8616a8-2eab-c85c-e063-6294a90a3984 2025-11-14 Warnings Exact identifier application number: M020 Naturium UV Reflect Antioxidant SPF 50 HOMOSALATE, OCTISALATE, AVOBENZONE e.l.f. Cosmetics, Inc 0a5c6fc8-6cdc-0ae5-e063-6394a90ae01c 2025-11-14 Warnings Exact identifier application number: M020 CERAVE DEVELOPED WITH DERMOTOLOGISTS Invisible Mineral Sunscreen FOR ALL SKIN TYPES AND TONES FACE UVB AND UVA BROAD SPECTRUM SPF 50 TITANIUM DIOXIDE AND ZINC OXIDE LOreal USA Products Inc 372894af-bed7-474f-95d4-69a8c3f215ef 2025-11-14 Warnings Exact identifier application number: M020 HEIMISH RX HYALURONIC ACID HYDRATING SUNSCREEN AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE ONEAND CO., LTD. 2dc41560-f4a7-5f0b-e063-6294a90a0630 2025-11-13 Warnings Exact identifier application number: M020 Covey Sun and Done Daily Moisturizing ZINC OXIDE Covey Skin fbcf8204-0673-99aa-e053-6294a90ac26e 2025-11-13 Warnings Exact identifier application number: M020 SOL Science The Fifty ZINC OXIDE Beauty Pie 01548858-8b0e-494a-e063-6294a90a8e99 2025-11-13 Warnings Exact identifier application number: M020 Balmere Mineral Sunscreen Moisturizer Primer ZINC OXIDE Balmere 00d813e0-eb97-a6ba-e063-6394a90aa525 2025-11-13 Warnings Exact identifier application number: M020 Dove Clinical Care 96H PROTECTION FRESH PEACH DRY SPRAY ANTIPERSPIRANT DEODORANT Conopco d/b/a Unilever 437eb2a8-428c-8339-e063-6394a90a74b2 2025-11-13 Warnings Exact identifier application number: M020 Dove Clinical Care 96H PROTECTION ORIGINAL CLEAN DRY SPRAY ANTIPERSPIRANT DEODORANT Conopco d/b/a Unilever 437f4db5-552f-1550-e063-6394a90aaedb 2025-11-13 Warnings Exact identifier application number: M020 Depology Essential Mineral UV Care ZINC OXIDE Depology Holdings LLC 1d48cdee-be67-14c0-e063-6294a90a7422 2025-11-13 Warnings Exact identifier application number: M020 Hanalei Face Moisturizing ZINC OXIDE Hanalei Beauty Company LLC 1f7c1a68-5aea-0deb-e063-6394a90a3a43 2025-11-13 Warnings Exact identifier application number: M020 Glo Skin TITANIUM DIOXIDE, ZINC OXIDE Glo Skin Beauty f4bed574-68c1-0d2c-e053-2a95a90a15ff 2025-11-13 Warnings Exact identifier application number: M020 Dove Clinical Care 96H PROTECTION SOFT SENSITIVE DRY SPRAY ANTIPERSPIRANT DEODORANT Conopco d/b/a Unilever 4380036a-7698-03e7-e063-6294a90a7301 2025-11-13 Warnings Exact identifier application number: M020 SOME BY MI V10 HYAL AIR FIT SUNSCREEN SUNSCREENT PERENNEBELL fe2148db-9020-9343-e053-6294a90adf70 2025-11-13 Warnings Exact identifier application number: M020 skin MD OCTINOXATE, OCTISALATE, HOMOSALATE 21st Century Formulations e809e1d3-0a6d-730d-e053-2a95a90aedb9 2025-11-13 Warnings 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