DIY Booster SPF 30 Facial Serum Unscented

Product NDC: 55560-0107
11-digit product format: 555600107
Labeler code: 55560
Product ID: 55560-0107_9a9818f7-62ad-4681-a456-f6158307085e
Type: HUMAN OTC DRUG
Nonproprietary name: Octinoxate, Octisalate, Avobenzone, and Zinc Oxide
Dosage form: LOTION
Route: TOPICAL
Labeler: Andalou naturals
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2014-03-01
Marketing end: 2027-03-31
Substance: OCTINOXATE; OCTISALATE; AVOBENZONE; ZINC OXIDE
Active strength: 70; 50; 30; 1 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag: No
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 · 22 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	55560-0107-1	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	55560-0107-1	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	55560-0107-1	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	55560-0107-1	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	55560-0107-1	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	55560-0107-1	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	55560-0107-1	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	55560-0107-1	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	55560-0107-1	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	55560-0107-1	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	55560-0107-1	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`

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: DIY Booster SPF 30 Facial Serum Unscented

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
OCTINOXATE	70 mg/mL
OCTISALATE	50 mg/mL
AVOBENZONE	30 mg/mL
ZINC OXIDE	1 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
4Y5P7MUD51	Internal UNII lookup
4X49Y0596W	Internal UNII lookup
G63QQF2NOX	Internal UNII lookup
SOI2LOH54Z	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
ebaf5ef7-84aa-4cb1-a701-2e0d0fd357df	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2025-06-09	DIY Booster SPF 30 Facial Serum Unscented
2025-01-30	DIY Booster SPF 30 Facial Serum Unscented
2023-02-02	DIY Booster SPF 30 Facial Serum Unscented
2021-01-29	DIY Booster SPF 30 Facial Serum Unscented

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55560-0107-1	DIY Booster SPF 30 Facial Serum Unscented	58 mL in 1 TUBE	LOTION	58		7
55560-0107-1	DIY Booster SPF 30 Facial Serum Unscented	1 in 1 CARTON	LOTION	1		7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55560-0107	DIY BOOSTER SPF 30 FACIAL SERUM UNSCENTED (OCTINOXATE, OCTISALATE, AVOBENZONE, AND ZINC OXIDE) LOTION [ANDALOU NATURALS]	4	Current NDC, Legacy NDC, 2 package rows	20230203_ebaf5ef7-84aa-4cb1-a701-2e0d0fd357df.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 65 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Tanning Club Mineral Sunscreen SPF 30	ZINC OXIDE	Tanning Club LLC	d674ccbc-7bae-435c-a531-a79e569e69a9	2026-02-04	Warnings	Exact identifier application number: M020
Derma B Everyday Fit Sunscreen SPF 50	AVOBEZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	NeoPharm Co., Ltd.	ba38a43d-7a8a-4814-ba34-0e99124f5fca	2026-02-04	Warnings	Exact identifier application number: M020
SHISEIDO URBAN ENVIRONMENT oil-free MINERAL SUNSCREEN SPF 42	TITANIUM DIOXIDE AND ZINC OXIDE	SHISEIDO AMERICAS CORPORATION	86630e82-f249-4866-82dd-3e21feb266c4	2026-02-04	Warnings	Exact identifier application number: M020
SHISEIDO URBAN ENVIRONMENT FRESH-MOISTURE SUNSCREEN SPF 42	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	SHISEIDO AMERICAS CORPORATION	42adc51f-f500-485d-82a0-126672141262	2026-02-04	Warnings	Exact identifier application number: M020
SHISEIDO URBAN ENVIRONMENT VITA-CLEAR SUNSCREEN	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	SHISEIDO AMERICAS CORPORATION	60e55ebb-47b8-465e-819a-af195952e1ca	2026-02-04	Warnings	Exact identifier application number: M020
SHISEIDO BENEFIANCE NUTRIPERFECT DAY	AVOBENZONE, OCTINOXATE, AND OCTOCRYLENE	SHISEIDO AMERICAS CORPORATION	f644c67b-3a71-411b-b321-39a8b18af0c7	2026-02-04	Warnings	Exact identifier application number: M020
cle de peau BEAUTE UV PROTECTIVE N	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Shiseido Americas Corporation	4b242b76-8aed-4939-9906-741828acd815	2026-02-04	Warnings	Exact identifier application number: M020
cle de peau BEAUTE PORE-REFINING MATTIFYING VEIL	AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE	Shiseido Americas Corporation	efcf240f-95cb-45e0-b58a-9c8f3609aa55	2026-02-04	Warnings	Exact identifier application number: M020
cle de peau BEAUTE PORE-REFINING MATTIFYING VEIL	AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE	Shiseido Americas Corporation	270ecc83-4262-4102-a753-2acaf11360a0	2026-02-04	Warnings	Exact identifier application number: M020
Walgreens 50 Caramel and Pistachio Scented Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	WALGREEN COMPANY	4a038017-9f15-b4b2-e063-6294a90a1b23	2026-02-04	Warnings	Exact identifier application number: M020
SHISEIDO ULTIMATE SUN PROTECTOR	OCTISALATE, OCTOCRYLENE, ZINC OXIDE	Shiseido Americas Corporation	ce6a28c1-56e6-4105-bc9d-9d1986ead420	2026-02-04	Warnings	Exact identifier application number: M020
Sport Sunscreen SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE	HARRIS TEETER	d52e2c61-edbc-4c26-b1a7-e8eb656db188	2026-02-04	Warnings, Adverse reactions	Exact identifier application number: M020
Sport Sunscreen SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE	HARRIS TEETER	d365ed6d-a92f-473b-be19-b8b63d17f3b7	2026-02-04	Warnings, Adverse reactions	Exact identifier application number: M020
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	HARRIS TEETER	0a3b4597-06fe-4689-9751-6577867d755e	2026-02-04	Warnings, Adverse reactions	Exact identifier application number: M020
Sport Sunscreen SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE	HARRIS TEETER	b83ea476-fa32-4405-9ae3-f294836edb62	2026-02-04	Warnings	Exact identifier application number: M020
Sunplus SPF50 Face Body Sunscreen	SUNSCREEN	I.Shay Cosmetics	26d55baf-66dc-b1b8-e063-6394a90a670d	2026-02-04	Warnings	Exact identifier application number: M020
NUDESCREEN DEWY ILLUMINATING GLOW SPF 30 - Angel Glow	ZINC OXIDE SUNSCREEN	Bentley Laboratories, LLC	351217c4-8d71-41d9-ab08-c43857c0510c	2026-02-04	Warnings	Exact identifier application number: M020
NIDA Invisible Fit Sun Stick	SUN STICK	Proso Corp	49eca4f2-aae3-a0d5-e063-6394a90ab25f	2026-02-03	Warnings	Exact identifier application number: M020
Shiny Hiny SPF 45 Mineral Sunscreen	ZINC OXIDE	Shiny Hiny Products, LLC	31adde36-5e1b-40ff-e063-6294a90a6f2e	2026-02-03	Warnings	Exact identifier application number: M020
Walgreens 50 Passion Fruit Scented Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	WALGREEN COMPANY	49f030d8-959c-a3cd-e063-6294a90ae1ba	2026-02-03	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4Y5P7MUD51	OCTINOXATE	83834-59-7	OCTINOXATE
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
G63QQF2NOX	AVOBENZONE	70356-09-1	AVOBENZONE
SOI2LOH54Z	ZINC OXIDE	1314-13-2	ZINC OXIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
55560-0107-1	55560010701	1 TUBE in 1 CARTON (55560-0107-1) / 58 mL in 1 TUBE	1 tube	2014-03-01	2027-03-31	No	No	Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
DIY Booster SPF 30 Facial Serum Unscented	Andalou naturals \| Sun Deep Inc	2026-03-12	HUMAN OTC DRUG LABEL	7