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.

Identifier, FDA.report destination table
Identifier	FDA.report destination
106a9608-f7a4-0f8c-e063-6394a90a26ab	Available on FDA.report

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 183 of 353 · 7,041 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
HAWAIIAN TROPIC	AVOBENZONE,OCTISALATE,OCTOCRYLENE	Edgewell Personal Care Brands LLC	053e76f0-8ca0-645d-e063-6394a90a01d2	2025-09-28	Warnings	Exact identifier application number: M020
Hawaiian Tropic Mineral Translucent Sunscreen Powder SPF 30	ZINC OXIDE	Edgewell Personal Care Brands LLC	cdc54f23-0efb-2fb4-e053-2995a90ae58b	2025-09-28	Warnings	Exact identifier application number: M020
HAWAIIAN TROPIC	AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE	Edgewell Personal Care Brands LLC	0540017a-52ac-7972-e063-6394a90a139c	2025-09-28	Warnings	Exact identifier application number: M020
HAWAIIAN TROPIC	AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE	Edgewell Personal Care Brands LLC	08f3b27f-b233-d406-e063-6394a90ada76	2025-09-28	Warnings	Exact identifier application number: M020
HAWAIIAN TROPIC	AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE	Edgewell Personal Care Brands LLC	128a3772-b9b7-0d10-e063-6294a90a3e05	2025-09-28	Warnings	Exact identifier application number: M020
HAWAIIAN TROPIC	AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE	Edgewell Personal Care Brands LLC	203c82a2-0131-8023-e063-6294a90aba7b	2025-09-28	Warnings	Exact identifier application number: M020
HAWAIIAN TROPIC	AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE	Edgewell Personal Care Brands LLC	203c780a-3107-d71a-e063-6394a90aca25	2025-09-28	Warnings	Exact identifier application number: M020
HAWAIIAN TROPIC	AVOBENZONE,OCTISALATE,OCTOCRYLENE	Edgewell Personal Care Brands LLC	31d01fae-4085-d84a-e063-6294a90ab981	2025-09-28	Warnings	Exact identifier application number: M020
Hawaiian Tropic	AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE	Edgewell Personal Care Brands, LLC	3388c2fa-8082-95d4-e063-6294a90a94b8	2025-09-28	Warnings	Exact identifier application number: M020
Neutrogena Beach Defense Water Plus Sun Protection Sunscreen Broad Spectrum SPF30	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE	Kenvue Brands LLC	b10a7794-7e4f-412b-9eb2-773107ecb7fc	2025-09-26	Warnings	Exact identifier application number: M020
Black Girl Sunscreen SPF 50	HOMOSALATE 10.00% OCTOCRYLENE 10.00% OCTISALATE 5.00% AVOBENZONE 3.00%	Black Girl Sunscreen	fed22570-e0ae-43e1-b6ce-1f0ad01684c3	2025-09-26	Warnings	Exact identifier application number: M020
Smooth Even Glow	TINTED SUNSCREEN BROAD SPF30	SKNVcare, LLC	3fa48151-fcb9-3d35-e063-6394a90a2eb6	2025-09-25	Warnings	Exact identifier application number: M020
CHEEK CREME BROAD SPECTRUM SPF 30 SUNSCREEN BLUSH HEAT WAVE	AVOBENZONE, HOMOSALATE, OCTISALATE	MDSolarSciences	3fa810b0-0211-f2a7-e063-6294a90a0b72	2025-09-25	Warnings	Exact identifier application number: M020
SUN BUFF SPF 30 MINERAL SUNSCREEN	ZINC OXIDE/TITANIUM DIOXIDE	SPF Ventures, LLC	3f874062-ebab-8993-e063-6294a90abfc5	2025-09-24	Warnings	Exact identifier application number: M020
HygieneLab Face and Body Mineral Sunscreen SPF 50	ZINC OXIDE	HYGIENELAB, INC	7db103da-b434-433a-a18f-a727165640c0	2025-09-24	Warnings	Exact identifier application number: M020
Eve Lom Daily Protection Broad Spectrum SPF 50 Sunscreen	HOMOSALATE, OCTISALATE, OXYBENZONE, AVOBENZONE, OCTINOXATE AND OCTOCRYLENE	Space Brands Limited	0e2c9ffb-036d-49c5-abdb-2ee8888df318	2025-09-24	Warnings	Exact identifier application number: M020
PUR 4-in-1 Skin Tint DG6	ZINC OXIDE	PUR Minerals	3f8e97a7-2023-ba9c-e063-6294a90ac9c9	2025-09-24	Warnings	Exact identifier application number: M020
PUR 4-in-1 Skin Tint TN7	ZINC OXIDE	PUR Minerals	3f0717c7-f43f-e3b1-e063-6394a90a74dd	2025-09-24	Warnings	Exact identifier application number: M020
PUR 4-in-1 Skin Tint TN2	ZINC OXIDE	PUR Minerals	3f06ed2f-f43f-53d4-e063-6294a90af0dd	2025-09-24	Warnings	Exact identifier application number: M020
PUR 4-in-1 Skin Tint MN4	ZINC OXIDE	PUR Minerals	3f06f618-f7b2-53d0-e063-6294a90a829c	2025-09-24	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
95OOS7VE0Y	OXYBENZONE	131-57-7	OXYBENZONE
4Y5P7MUD51	OCTINOXATE	83834-59-7	OCTINOXATE

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