Daily Facial Moisturizer

Product NDC: 0096-0721
11-digit product format: 000960721
Labeler code: 0096
Product ID: 0096-0721_4bac1be4-bde9-8a04-e063-6394a90a438e
Type: HUMAN OTC DRUG
Nonproprietary name: Sunscreen
Dosage form: CREAM
Route: TOPICAL
Labeler: Person and Covey
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1991-08-01
Substance: HOMOSALATE; AVOBENZONE; OCTINOXATE; OCTOCRYLENE
Active strength: .06; .03; .075; .015 g/g; g/g; g/g; g/g
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	0096-0721	0096-0721-07	D	Discontinued by firm		2026-10-21

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
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	0096-0721-07	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	0096-0721-07	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	0096-0721-07	D	Discontinued by firm	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	0096-0721-07	D	Discontinued by firm	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	0096-0721-07	D	Discontinued by firm	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	0096-0721-07	D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
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	0096-0721-45	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	0096-0721-07	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	0096-0721-45	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	0096-0721-07	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	0096-0721-45	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	0096-0721-07	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	0096-0721-45	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	0096-0721-07	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded product	product		I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	0096-0721-45	I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	0096-0721-07	I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded product	product		I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	0096-0721-45	I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	0096-0721-07	I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`

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: Daily Facial Moisturizer
Brand name suffix: SPF 25
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
HOMOSALATE	.06 g/g
AVOBENZONE	.03 g/g
OCTINOXATE	.075 g/g
OCTOCRYLENE	.015 g/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
V06SV4M95S	Internal UNII lookup
G63QQF2NOX	Internal UNII lookup
4Y5P7MUD51	Internal UNII lookup
5A68WGF6WM	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
6b9258e4-c7c6-765e-e053-2991aa0a9f4e	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
0096-0721-07	2024-02-27	DML Daily Facial Moisturizer
0096-0721-07	2024-02-27	DML Daily Facial Moisturizer
0096-0721-07	2024-02-27	DML Daily Facial Moisturizer
0096-0721-07	2024-02-27	DML Daily Facial Moisturizer
0096-0721-07	2024-02-27	DML Daily Facial Moisturizer
0096-0721-45	2024-02-27	DML Daily Facial Moisturizer
0096-0721-45	2024-02-27	DML Daily Facial Moisturizer
0096-0721-45	2024-02-27	DML Daily Facial Moisturizer
0096-0721-45	2024-02-27	DML Daily Facial Moisturizer
0096-0721-45	2024-02-27	DML Daily Facial Moisturizer
0096-0721-07	2020-01-31	DML Daily Facial Moisturizer
0096-0721-07	2020-01-31	DML Daily Facial Moisturizer
0096-0721-07	2020-01-31	DML Daily Facial Moisturizer
0096-0721-07	2020-01-31	DML Daily Facial Moisturizer
0096-0721-07	2020-01-31	DML Daily Facial Moisturizer
0096-0721-45	2020-01-31	DML Daily Facial Moisturizer
0096-0721-45	2020-01-31	DML Daily Facial Moisturizer
0096-0721-45	2020-01-31	DML Daily Facial Moisturizer
0096-0721-45	2020-01-31	DML Daily Facial Moisturizer
0096-0721-45	2020-01-31	DML Daily Facial Moisturizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0096-0721-07	Daily Facial MoisturizerSPF 25	7 g in 1 BOTTLE	CREAM	7	9
0096-0721-10	Daily Facial MoisturizerSPF 25	10 g in 1 TUBE	CREAM	10	9
0096-0721-45	Daily Facial MoisturizerSPF 25	45 g in 1 BOTTLE	CREAM	45	9

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0096-0721-45	GM - Gram	0096-0721	4f4b0ce4-60b7-4848-9612-3b527cfc01bf	1	2018-08-13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0096-0721	DAILY FACIAL MOISTURIZER SPF 25 (SUNSCREEN) CREAM [PERSON AND COVEY]	5	Current NDC, Legacy NDC, 3 package rows	20250221_6b9258e4-c7c6-765e-e053-2991aa0a9f4e.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 54 of 354 · 7,077 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	Nice-Pak Products, LLC	af052521-bfa6-4142-a10b-ef51f474a077	2026-03-13	Warnings, Adverse reactions	Exact identifier application number: M020
Moisturizing Sunscreen SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE	Nice-Pak Products, LLC	42647444-93a3-4d2c-9bfc-91621fd098f7	2026-03-13	Warnings, Adverse reactions	Exact identifier application number: M020
Sunscreen for Babies SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE	Nice-Pak Products, LLC	a4b9d7c0-dc09-4f0e-8b65-90ba180552bf	2026-03-13	Warnings, Adverse reactions	Exact identifier application number: M020
TINTED WATERY SUNSCREEN	TITANIUM DIOXIDE, ZINC OXIDE	KSISTERS PTE. LTD.	4ced53d0-8bfc-ff8e-e063-6294a90a9dbd	2026-03-13	Warnings	Exact identifier application number: M020
Round Lab Birch Juice Mother s Day Gift Set	AVOBENZONE, HOMOSALATE, OCTISALATE	SEORIN COMPANY Co., Ltd.	4cf03092-7886-ffa1-e063-6294a90a2aad	2026-03-13	Warnings	Exact identifier application number: M020
Daily Moisturizing Mineral Sunscreen	BROAD SPECTRUM SPF30	EDINA PLASTIC SURGERY,LTD.	4d056e2b-5813-da42-e063-6294a90ac519	2026-03-13	Warnings	Exact identifier application number: M020
La Roche Posay Anthelios Sunscreen SPF 60 Ultra light	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE	L'Oreal USA, Inc.	dad00eee-92cd-7610-e053-2a95a90a1fac	2026-03-13	Warnings	Exact identifier application number: M020
VITARAN REJUVENA SUNCARE	ALLANTOIN, AVOBENZONE, HOMOSALATE, OCTISALATE	BR PHARM CO. , Ltd.	4cb7af72-49f6-0738-e063-6394a90a79eb	2026-03-12	Warnings	Exact identifier application number: M020
MIZON SNAIL REPAIR INTENSIVE BB No. 21	ZINC OXIDE, OCTISALATE, OCTOCRYLENE	PFD Co.,Ltd.	4cd0a8a7-11aa-e168-e063-6394a90a2ff2	2026-03-12	Warnings	Exact identifier application number: M020
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	Vi-Jon, LLC	3da4706e-7c1a-435e-9603-e9aa98432018	2026-03-12	Warnings, Adverse reactions	Exact identifier application number: M020
Sunscreen SPF50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Nice-Pak Products, LLC	53806657-7b4d-45ff-a75b-9340dcd8140e	2026-03-12	Warnings, Adverse reactions	Exact identifier application number: M020
Sunscreen SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Nice-Pak Products, LLC	08237b4c-4e5c-4b12-9510-2f8d64ab7f3a	2026-03-12	Warnings, Adverse reactions	Exact identifier application number: M020
SunnyDays Broad Spectrum SPF 30 Tinted Sunscreen 5 Fairfax	ZINC OXIDE	Tower 28	108851ac-3812-4c02-a04a-9f9a7f529ed6	2026-03-12	Warnings	Exact identifier application number: M020
DIY Booster SPF 30 Facial Serum Unscented	OCTINOXATE, OCTISALATE, AVOBENZONE, AND ZINC OXIDE	Andalou naturals	ebaf5ef7-84aa-4cb1-a701-2e0d0fd357df	2026-03-12	Warnings	Exact identifier application number: M020
Vacation SPF 50 Classic	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Vacation INC.	f268fb1c-d7c2-f2f9-e053-2995a90a9e22	2026-03-12	Warnings	Exact identifier application number: M020
Neutrogena Healthy Skin Liquid Makeup Broad Spectrum SPF 20 - Cool Bronze 440C	TITANIUM DIOXIDE	Kenvue Brands LLC	4c335d9c-40ca-c0ce-e063-6394a90ac20a	2026-03-11	Warnings	Exact identifier application number: M020
CENTELLA SUNSCREEN Cream	ZINC OXIDE	Yunqi Cosmetics (Shenzhen) Co., Ltd	4cbac4e9-7540-f703-e063-6394a90ad808	2026-03-11	Warnings	Exact identifier application number: M020
Vacation Lip Balm	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	Vacation INC.	4ba8ed52-2f52-40b9-a810-8450f9b90778	2026-03-10	Warnings	Exact identifier application number: M020
COOLA Zinc Oxide BodyLotion SPF 50 Fragrance-Free	ZINC OXIDE	COOLA LLC	4cad89a5-325c-b3c2-e063-6294a90ac225	2026-03-10	Warnings	Exact identifier application number: M020
Olay Complete plus Facial Moisturizer with Sunscreen Broad Spectrum SPF 40 Sensitive	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	The Procter & Gamble Manufacturing Company	4caf2ab5-76cb-4b0f-e063-6294a90a233e	2026-03-10	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
G63QQF2NOX	AVOBENZONE	70356-09-1	AVOBENZONE
4Y5P7MUD51	OCTINOXATE	83834-59-7	OCTINOXATE
5A68WGF6WM	OCTOCRYLENE	6197-30-4	OCTOCRYLENE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
0096-0721-07	00096072107	7 g in 1 BOTTLE	7 g				Historical
0096-0721-10	00096072110	10 g in 1 TUBE (0096-0721-10)	10 g	2026-02-23	Yes	No	Current
0096-0721-45	00096072145	45 g in 1 BOTTLE (0096-0721-45)	45 g	1991-08-01	No	No	Current