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 226 of 346 · 6,912 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Dr Loretta Universal Glow Daily Defense SPF 40	ZINC OXIDE	Dr. Loretta, LLC	ebdaf6c1-1572-4840-851b-6d780471fcb2	2025-02-11	Warnings	Exact identifier application number: M020
Sky and Sol Body Sunscreen SPF50	SKY AND SOL BODY SUNSCREEN SPF50	Guangzhou Fantesy Biotechnology Co.,Ltd	2de9173b-fa02-8017-e063-6394a90ae0aa	2025-02-11	Warnings	Exact identifier application number: M020
Beeswax SPF 15 Broad Spectrum Lip Balm	BEESWAX SPF 15 BROAD SPECTRUM LIP BALM	Raining Rose, Inc	2dcc2f9b-4a8c-b281-e063-6294a90ad9d6	2025-02-10	Warnings	Exact identifier application number: M020
Broad Spectrum SPF 30 Tropical Sunscreen	BROAD SPECTRUM SPF 30 TROPICAL SUNSCREEN	Raining Rose, Inc	2dcca380-c0e4-4e04-e063-6394a90ac31e	2025-02-10	Warnings	Exact identifier application number: M020
Artistry Ideal Radiance Illuminating CC SPF 50 Broad Spectrum Sunscreen Deep	ENSULIZOLE, OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE	Amway Corp	88021a24-d3b5-48f8-8d26-affbfcfd098f	2025-02-10	Warnings	Exact identifier application number: M020
Sun Defense Minerals (Sheer)	ZINC OXIDE, TITANIUM DIOXIDE	Eminence Organic Skin Care	2dd20800-2cf9-02d4-e063-6294a90a0f00	2025-02-10	Warnings	Exact identifier application number: M020
Bondi Sands Fragrance Free Face SPF 50 Sunscreen Mist	HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE	BONDI SANDS (USA) INC.	2dd5ea23-eee6-5d14-e063-6294a90a0fd3	2025-02-10	Warnings	Exact identifier application number: M020
Centella Calming SUNSCREEN	CENTELLA CALMING SUNSCREEN	GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd	2dc0ee9b-d58b-fe40-e063-6394a90af439	2025-02-09	Warnings	Exact identifier application number: M020
SOME BY MI V10 HYAL LIP SUN PROTECTOR ROSY	AVOBENZONE, HOMOSALATE, OCTISALATE	PERENNEBELL Co., Ltd	2dc25afb-a171-f1f2-e063-6294a90ae333	2025-02-09	Warnings	Exact identifier application number: M020
SOME BY MI V10 HYAL LIP SUN PROTECTOR BERRY	AVOBENZONE, HOMOSALATE, OCTISALATE	PERENNEBELL Co., Ltd	2dc285ad-08cd-14e6-e063-6294a90a24fc	2025-02-09	Warnings	Exact identifier application number: M020
PROBIOTIC RICE Sunscreen	PROBIOTIC RICE SUNSCREEN	GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd	2d9d6440-39b3-312a-e063-6394a90aa072	2025-02-08	Warnings	Exact identifier application number: M020
NIA 24 SPF 30	HOMOSALATE, OCTISALATE, AVOBENZONE, OCTOCRYLENE	Niadyne Inc	e5c9d56f-48b4-4f0e-add6-f73268755b16	2025-02-07	Warnings	Exact identifier application number: M020
Pacific Mango Sunscreen SPF 30	AVOBENZONE, OCTISALATE, OCTOCRYLENE	SAN DIEGO NATURAL SOAP COMPANY	d09e3096-0678-4433-a555-61f18a45873b	2025-02-06	Warnings	Exact identifier application number: M020
DR.JART CICAPAIR TIGER GRASS COLOR CORRECTING TREATMENT	ZINC OXIDE, TITANIUM DIOXIDE	Have & Be Co., Ltd.	01cfe6a6-c2e4-8fb8-e063-6294a90adc78	2025-02-06	Warnings	Exact identifier application number: M020
Dr.Jart Premium Beauty Balm Medium-Tan	ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	Have & Be Co., Ltd.	02a8bab8-ca5d-6b65-e063-6294a90abb07	2025-02-06	Warnings	Exact identifier application number: M020
Dr.Jart Premium Beauty Balm Fair-Light	ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	Have & Be Co., Ltd.	02a82029-bdb1-cbe0-e063-6294a90a08f3	2025-02-06	Warnings	Exact identifier application number: M020
Dr.Jart Premium Beauty Balm Light Medium-Medium	ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	Have & Be Co., Ltd.	02a87c6b-3c7d-5942-e063-6294a90aa452	2025-02-06	Warnings	Exact identifier application number: M020
DR.JART EVERY SUN DAY MINERAL SUN SCREEN	TITANIUM DIOXIDE, ZINC OXIDE	Have & Be Co., Ltd.	02a671ed-485d-d6b7-e063-6394a90ad4af	2025-02-06	Warnings	Exact identifier application number: M020
Dr.Jart Cicapair Tiger Grass Camo Drops	ZINC OXIDE, TITANIUM DIOXIDE	Have & Be Co., Ltd.	01cf0522-a3c1-aea8-e063-6294a90aabfe	2025-02-06	Warnings	Exact identifier application number: M020
DR.JART EVERY SUN DAY SUN FLUID	HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE	Have & Be Co., Ltd.	02a72c6d-da42-14b2-e063-6394a90af5cb	2025-02-06	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