Voupre Age Defense

Product NDC: 72104-890
11-digit product format: 721040890
Labeler code: 72104
Product ID: 72104-890_c94114d1-f9c5-4048-b6da-ad415e382974
Type: HUMAN OTC DRUG
Nonproprietary name: Octinoxate, Homosalate, Octisalate, Oxybenzone and Avobenzone
Dosage form: CREAM
Route: TOPICAL
Labeler: Innovation Brands Inc.
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-07-27
Substance: OCTINOXATE; HOMOSALATE; OCTISALATE; OXYBENZONE; AVOBENZONE
Active strength: 7.4; 6.2; 5; 3.1; 1.5 g/100g; g/100g; g/100g; g/100g; g/100g
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 · 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	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	72104-890-52	D	Discontinued by firm	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	72104-890-09	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	72104-890-52	D	Discontinued by firm	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	72104-890-09	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	72104-890-52	D	Discontinued by firm	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	72104-890-09	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	72104-890-52	D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	72104-890-09	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	72104-890-52	D	Discontinued by firm	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	72104-890-09	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	72104-890-52	D	Discontinued by firm	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	72104-890-09	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	72104-890-52	D	Discontinued by firm	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	72104-890-09	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	72104-890-52	D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	72104-890-52	D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	72104-890-52	D	Discontinued by firm	`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: Voupre Age Defense
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
OCTINOXATE	7.4 g/100g
HOMOSALATE	6.2 g/100g
OCTISALATE	5 g/100g
OXYBENZONE	3.1 g/100g
AVOBENZONE	1.5 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 5 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
4Y5P7MUD51	Internal UNII lookup
V06SV4M95S	Internal UNII lookup
4X49Y0596W	Internal UNII lookup
95OOS7VE0Y	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
8dfaa076-c62a-47ee-bc5d-75360416fa1a	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
72104-890-09	2025-06-17	Voupre ® Age Defense Cream
72104-890-52	2025-06-17	Voupre ® Age Defense Cream
72104-890-09	2025-01-30	Voupre ® Age Defense Cream
72104-890-52	2025-01-30	Voupre ® Age Defense Cream
72104-890-52	2022-08-09	Voupre ® Age Defense Cream
72104-890-52	2022-07-29	Voupre ® Age Defense Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72104-890-09	Voupre Age Defense	1 in 1 CARTON	CREAM	1		4
72104-890-09	Voupre Age Defense	65 g in 1 JAR	CREAM	65		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72104-890	VOUPRE AGE DEFENSE (OCTINOXATE, HOMOSALATE, OCTISALATE, OXYBENZONE AND AVOBENZONE) CREAM [LIONESSE USA, INC.]	3	Current NDC, Legacy NDC, 2 package rows	20230707_8dfaa076-c62a-47ee-bc5d-75360416fa1a.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 145 of 353 · 7,041 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Mineral Lip Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	ASHLEY SAMAI	38f457fa-0e95-7298-e063-6394a90adda8	2025-12-09		Exact identifier application number: M020
Non-Tinted Mineral Sunscreen	ZINC OXIDE	OLGA KLIMOV INC	387b41a4-057f-88af-e063-6394a90adbbe	2025-12-09		Exact identifier application number: M020
Tinted Replenishing Daily Protection	ZINC OXIDE	OLGA KLIMOV INC	387b8ae6-c48b-905c-e063-6394a90a31fb	2025-12-09		Exact identifier application number: M020
Tinted Primer Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	CECILIA EDWARDS	36ea709b-3536-5052-e063-6394a90a48f9	2025-12-09		Exact identifier application number: M020
Age Defying Mineral Protection	TITANIUM DIOXIDE, ZINC OXIDE	MARK SCHWARTZ CLINICAL SKINCARE, INC.	3b028159-f240-2cf2-e063-6294a90a32b5	2025-12-09	Warnings	Exact identifier application number: M020
Ultimate Mineral Protection	ZINC OXIDE	MARK SCHWARTZ CLINICAL SKINCARE, INC.	3b02bf69-b648-56e1-e063-6294a90aeef3	2025-12-09	Warnings	Exact identifier application number: M020
G.M. Collin FPS-SPF 45 UVA-UVB TINTED SUNSCREEN	ZINC OXIDE, TITANIUM DIOXIDE	LABORATOIRES DERMO-COSMETIK INC.	01dcfd14-7a1d-98fa-e063-6294a90a0336	2025-12-09	Warnings	Exact identifier application number: M020
Tinted Primer Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	CECILIA EDWARDS	3aff2074-1514-b5c5-e063-6394a90a7572	2025-12-09		Exact identifier application number: M020
Mineral Lip Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER	3729d270-64ac-4d2e-e063-6294a90aeb2c	2025-12-09		Exact identifier application number: M020
Non Tinted Replenishing Daily Protection	ZINC OXIDE	LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER	372a41f6-40f6-4971-e063-6394a90a83e0	2025-12-09		Exact identifier application number: M020
Stay Shady Non-Tinted Mineral Sunscreen	ZINC OXIDE	AMOIE ALAYVILLA	3b277237-3a2e-1fb0-e063-6294a90adf20	2025-12-09	Warnings	Exact identifier application number: M020
Stay Shady Non-Tinted Mineral Sunscreen	ZINC OXIDE	AMOIE ALAYVILLA	3b27225f-4589-d915-e063-6294a90a7225	2025-12-09	Warnings	Exact identifier application number: M020
Replenishing Tinted Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Beauty Journey Studio LLC	3738a0c3-5c07-e49b-e063-6394a90a38e9	2025-12-09		Exact identifier application number: M020
Replenishing Non Tinted Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Beauty Journey Studio LLC	37385fc6-1cde-8aa6-e063-6294a90a6017	2025-12-09		Exact identifier application number: M020
Replenishing Tinted Sunscreen	ZINC OXIDE	Beauty Journey Studio LLC	3738e5e0-f6d9-0568-e063-6294a90a67b6	2025-12-09		Exact identifier application number: M020
JAYSUING Matte Sun Stick	TITANIUM DIOXIDE	Shantou Jaysuing Cleaning and Environmental Protection Technology Co., Ltd.	456b44da-02f3-93a0-e063-6294a90a8d06	2025-12-08	Warnings	Exact identifier application number: M020
JAYSUING Matte Sun Stick	TITANIUM DIOXIDE	Shantou Jaysuing Cleaning and Environmental Protection Technology Co., Ltd.	456c2974-d499-7841-e063-6294a90a98eb	2025-12-08	Warnings	Exact identifier application number: M020
JAYSUING Ginseng Moist Sun Serum	TITANIUM DIOXIDE	Shantou Jaysuing Cleaning and Environmental Protection Technology Co., Ltd.	456cfa70-f524-f5cb-e063-6394a90ae7dc	2025-12-08	Warnings	Exact identifier application number: M020
Face and Body Sunscreen	NON-NANO ZINC OXIDE 25%	Guangzhou Shengyanghui Industrial Trading Co., Ltd	3ee96538-06e8-75b1-e063-6394a90a5285	2025-12-08	Warnings	Exact identifier application number: M020
Safe Sea SPF sport 65	HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE	NIDARIA TECHNOLOGY LTD	0ed3242b-ac35-4d98-a777-1e44bb32a467	2025-12-08	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
V06SV4M95S	HOMOSALATE	118-56-9	HOMOSALATE
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
95OOS7VE0Y	OXYBENZONE	131-57-7	OXYBENZONE
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
72104-890-09	72104089009	1 JAR in 1 CARTON (72104-890-09) / 65 g in 1 JAR	1 jar	2023-10-01		No	No	Current
72104-890-52	72104089052	1 JAR in 1 CARTON (72104-890-52) > 50 g in 1 JAR	1 jar	2021-07-27	0000-00-00	No	No	Current