ULTRA SHEER DAILY DEFENSE FACIAL SPF 18

Product NDC: 55560-3331
11-digit product format: 555603331
Labeler code: 55560
Product ID: 55560-3331_258b9705-1493-4410-9bb6-49cf7977eea8
Type: HUMAN OTC DRUG
Nonproprietary name: Homosalate, Octisalate, and Avobenzone
Dosage form: LOTION
Route: TOPICAL
Labeler: Andalou naturals
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-01-01
Substance: HOMOSALATE; OCTISALATE; AVOBENZONE
Active strength: 120; 40; 30 mg/mL; mg/mL; mg/mL
NDC exclude flag: No
Listing certified through: 2026-12-31
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 · 14 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	55560-3331-1	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	55560-3331-1	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	55560-3331-1	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	55560-3331-1	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	55560-3331-1	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	55560-3331-1	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	55560-3331-1	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

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: ULTRA SHEER DAILY DEFENSE FACIAL SPF 18
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
HOMOSALATE	120 mg/mL
OCTISALATE	40 mg/mL
AVOBENZONE	30 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
V06SV4M95S	Internal UNII lookup
4X49Y0596W	Internal UNII lookup
G63QQF2NOX	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
0f7c6d3a-73ea-44d8-a8b9-6a6f1bb02c6f	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
7792dadb-52b6-46b6-8fdf-80b1171065b5	Product name	1	20180810

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2025-06-11	ULTRA SHEER DAILY DEFENSE FACIAL SPF 18
2025-01-30	ULTRA SHEER DAILY DEFENSE FACIAL SPF 18
2023-02-02	ULTRA SHEER DAILY DEFENSE FACIAL SPF 18
2023-01-30	ULTRA SHEER DAILY DEFENSE FACIAL SPF 18

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55560-3331-1	ULTRA SHEER DAILY DEFENSE FACIAL SPF 18	80 mL in 1 TUBE	LOTION	80		5
55560-3331-1	ULTRA SHEER DAILY DEFENSE FACIAL SPF 18	1 in 1 BOX	LOTION	1		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55560-3331	ULTRA SHEER DAILY DEFENSE FACIAL SPF 18 (HOMOSALATE, OCTISALATE, AND AVOBENZONE) LOTION [ANDALOU NATURALS]	3	Current NDC, Legacy NDC, 2 package rows	20230203_0f7c6d3a-73ea-44d8-a8b9-6a6f1bb02c6f.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 8 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ceile tint PROTECT tinted serum SPF 50 Ivory	CEILE TINT PROTECT TINTED SERUM SPF 50 IVORY	LE COSMETICS INC	58547809-3480-1032-e063-6294a90a04c6	2026-08-05	Warnings	Exact identifier application number: M020
Ceile tint PROTECT tinted serum SPF 50 Medium Deep	CEILE TINT PROTECT TINTED SERUM SPF 50 MEDIUM DEEP	LE COSMETICS INC	58549160-3594-9056-e063-6394a90abf7d	2026-08-05	Warnings	Exact identifier application number: M020
Ceile tint PROTECT tinted serum SPF 50 Deep	CEILE TINT PROTECT TINTED SERUM SPF 50 DEEP	LE COSMETICS INC	585498d4-b29c-9580-e063-6394a90adf1e	2026-08-05	Warnings	Exact identifier application number: M020
Ceile tint PROTECT tinted serum SPF 50 Fair	CEILE TINT PROTECT TINTED SERUM SPF 50 FAIR	LE COSMETICS INC	58545633-cb36-6611-e063-6394a90a1f07	2026-08-05	Warnings	Exact identifier application number: M020
Ceile tint PROTECT tinted serum SPF 50 Light	CEILE TINT PROTECT TINTED SERUM SPF 50 LIGHT	LE COSMETICS INC	5853ae6b-0eaf-e614-e063-6394a90ae91a	2026-08-05	Warnings	Exact identifier application number: M020
Ceile tint PROTECT tinted serum SPF 50 Light Medium	CEILE TINT PROTECT TINTED SERUM SPF 50 LIGHT MEDIUM	LE COSMETICS INC	585473c3-3ee9-7d84-e063-6394a90abd33	2026-08-05	Warnings	Exact identifier application number: M020
Ceile tint PROTECT tinted serum SPF 50 Medium	CEILE TINT PROTECT TINTED SERUM SPF 50 MEDIUM	LE COSMETICS INC	58547b48-251a-10eb-e063-6294a90ac95c	2026-08-05	Warnings	Exact identifier application number: M020
Ceile tint PROTECT tinted serum SPF 50 Medium Tan	CEILE TINT PROTECT TINTED SERUM SPF 50 MEDIUM TAN	LE COSMETICS INC	58547e38-ae84-82ee-e063-6394a90a27d6	2026-08-05	Warnings	Exact identifier application number: M020
Ceile tint PROTECT tinted serum SPF 50 Tan	CEILE TINT PROTECT TINTED SERUM SPF 50 TAN	LE COSMETICS INC	58548331-38cd-8668-e063-6394a90a3362	2026-08-05	Warnings	Exact identifier application number: M020
Ceile tint PROTECT tinted serum SPF 50 Medium Honey	CEILE TINT PROTECT TINTED SERUM SPF 50 MEDIUM HONEY	LE COSMETICS INC	5854861a-376d-8825-e063-6394a90a8aab	2026-08-05	Warnings	Exact identifier application number: M020
Ceile tint PROTECT tinted serum SPF 50 Honey	CEILE TINT PROTECT TINTED SERUM SPF 50 HONEY	LE COSMETICS INC	585488c5-fac5-212f-e063-6294a90a00ff	2026-08-05	Warnings	Exact identifier application number: M020
Ceile tint PROTECT tinted serum SPF 50 Medium Rich	CEILE TINT PROTECT TINTED SERUM SPF 50 MEDIUM RICH	LE COSMETICS INC	585488af-d14f-8d71-e063-6394a90ac4f0	2026-08-05	Warnings	Exact identifier application number: M020
Ceile tint PROTECT tinted serum SPF 50 Rich	CEILE TINT PROTECT TINTED SERUM SPF 50 RICH	LE COSMETICS INC	58548e6d-9c82-249c-e063-6294a90a11ad	2026-08-05	Warnings	Exact identifier application number: M020
12 Days of Derm-Loved Skincare	OCTINOXATE, ZINC OXIDE, OATMEAL, BENZOYL PEROXIDE, AVOBENZONE, OCTISALATE, OCTOCRYLENE	Rodan & Fields	a13f0275-5add-4464-88d4-ff9823274325	2026-08-03	Warnings	Exact identifier application number: M020
Luxe Gloss Hydrating Lip Gloss SPF 35-NAKED HONEY	OCTOCRYLENE 8%, OCTISALATE 5%, TITANIUM DIOXIDE 6%, ZINC OXIDE 8%	Lale Cosmetics LLC	581fb0cd-c55d-d562-e063-6394a90a7f11	2026-08-03	Warnings	Exact identifier application number: M020
Manyo Air Light Moisturizing Sunscreen SPF 50	ENSULIZOLE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Manyo Factory Corp.	86761577-a32c-41a2-a2e3-b339b1493701	2026-08-03	Warnings	Exact identifier application number: M020
EltaMD UV Active	ZINC OXIDE AND TITANIUM DIOXIDE SUNSCREEN	CP Skin Health Group, Inc	39d16479-d491-4c19-aa11-674461687c7b	2026-08-03	Warnings	Exact identifier application number: M020
AMBI SKINCARE Even and Clear Daily Facial Moisturizer SPF 30	OCTISALATE, OCTOCRYLENE, AVOBENZONE	AMBI Enterprises LLC	99bbe9a2-bb57-4a33-b339-1649d4b319c8	2026-07-31	Warnings	Exact identifier application number: M020
AMBI Even and Clear Facial Moisturizer SPF-30	AVOBENZONE, OCTISALATE, OCTOCRYLENE	AMBI Enterprises LLC	4701c0ba-4ceb-4d66-9f99-515ce33b4648	2026-07-31	Warnings	Exact identifier application number: M020
Continuous Correction Cream	TITANIUM DIOXIDE	Baxter of California, LLC	1cbcc648-f2e1-af60-e063-6294a90ad4bb	2026-07-31	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
V06SV4M95S	HOMOSALATE	118-56-9	HOMOSALATE
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
G63QQF2NOX	AVOBENZONE	70356-09-1	AVOBENZONE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
55560-3331-1	55560333101	1 TUBE in 1 BOX (55560-3331-1) / 80 mL in 1 TUBE	1 tube	2021-01-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
ULTRA SHEER DAILY DEFENSE FACIAL SPF 18	Andalou naturals \| Sun Deep Inc	2025-06-11	HUMAN OTC DRUG LABEL	5