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 85 of 354 · 7,077 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Daily Dose Bioretinol Mineral SPF 40	ZINC OXIDE	Supergoop, LLC	eb5bbc70-dbdf-06a8-e053-2995a90a66c1	2026-01-09	Warnings	Exact identifier application number: M020
Unseen Sunscreen Body SPF 40	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	ec1c30bd-76e1-9d00-e053-2a95a90a1759	2026-01-09	Warnings	Exact identifier application number: M020
Glow Screen SPF 40	AVOBENZONE, OCTISALATE, OCTOCYLENE	Supergoop, LLC	21569637-332a-461b-bf6c-33af6a83a155	2026-01-09	Warnings	Exact identifier application number: M020
Glowscreen SPF 40 - Dawn	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	f07145d5-b74d-7757-e053-2a95a90ac4c0	2026-01-09	Warnings	Exact identifier application number: M020
Glowscreen SPF 40 -Sunset	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	f7e493da-8fc6-191d-e053-6294a90aa483	2026-01-09	Warnings	Exact identifier application number: M020
Supergoop Glow Screen SPF 40 Shade 2 Golden Hour	BROAD SPECTRUM SUNSCREEN	Supergoop LLC	d2928dd7-a813-4929-e053-2a95a90aaeb4	2026-01-09	Warnings	Exact identifier application number: M020
Superscreen Hydrating Daily Cream SPF 40	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	ff0e4e97-8f01-bd36-e053-6394a90a47ae	2026-01-09	Warnings	Exact identifier application number: M020
Lipshade SPF 30 Hey Yall	ZINC OXIDE	Supergoop, LLC	f93dfa13-ff18-ee38-e053-6394a90aea46	2026-01-09	Warnings	Exact identifier application number: M020
Triple Prep SPF 40	AVOBENZONE, OCTISALATE, OCTOCRYLENE, HOMOSALATE	Supergoop, LLC	004df4e5-dba9-6030-e063-6394a90a76d3	2026-01-09	Warnings	Exact identifier application number: M020
Unseen Sunscreen Lip Protector SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	12605fb4-0de6-94f3-e063-6294a90a3a6f	2026-01-09	Warnings	Exact identifier application number: M020
Unseen Sunscreen Stick SPF 40	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	2735c5c7-a4ef-33c3-e063-6294a90abf97	2026-01-09	Warnings	Exact identifier application number: M020
PLAY Sunscreen SPF 50	HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE	Supergoop LLC	2860d42c-d644-8b5a-e063-6394a90aec10	2026-01-09	Warnings	Exact identifier application number: M020
PLAY Mineral SPF 30 with Green Algae	ZINC OXIDE	Supergoop LLC	29a1ff4b-3875-5275-e063-6394a90a53fd	2026-01-09	Warnings	Exact identifier application number: M020
Every. Single. Face. Watery SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	d086a9b8-19e5-f713-e053-2995a90aa976	2026-01-09	Warnings	Exact identifier application number: M020
3D Tinted Moisturizing BS SPF 30	ZINC OXIDE	Allure Labs	47fd415f-819e-bbb8-e063-6394a90a2c6a	2026-01-09	Warnings	Exact identifier application number: M020
ST MORIZ SUNCARE BODY SUNSCREEN SPF50	SUNCARE BODY SUNSCREEN SPF50	Aopline Biotechnology (Guangzhou) Co., Ltd.	4801cfd2-1fe2-d118-e063-6294a90a6c8b	2026-01-09	Warnings	Exact identifier application number: M020
ST MORIZ SUNCARE BODY SUNSCREEN SPF30	SUNCARE BODY SUNSCREEN SPF30	Aopline Biotechnology (Guangzhou) Co., Ltd.	48026f09-6d15-8fa6-e063-6294a90a17cb	2026-01-09	Warnings	Exact identifier application number: M020
RODAN and FIELDS ENHANCEMENTS MEDIUM	TITANIUM DIOXIDE, ZINC OXIDE	Bentley Laboratories, LLC	6aa6ad3f-2c52-4031-9e6c-7526c42de71d	2026-01-09	Warnings	Exact identifier application number: M020
FACE SPF 47 SETTING	FACE SPF 47 SETTING SPRAY	Aopline Biotechnology (Guangzhou) Co., Ltd.	47db9a54-c02f-d2ea-e063-6394a90ab973	2026-01-08	Warnings	Exact identifier application number: M020
BADABOOM SUNSCREEN	SUNSCREEN	Aopline Biotechnology (Guangzhou) Co., Ltd.	47dbf363-2892-4530-e063-6294a90abe1f	2026-01-08	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