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		2026-10-23

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 82 of 353 · 7,049 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Blue Lizard Baby SPF 50	ZINC OXIDE	Crown Laboratories	9948f5b8-43bd-1c99-e053-2a95a90a6121	2026-01-12	Warnings	Exact identifier application number: M020
Blue Lizard Sheer SPF 50 Sunscreen	ZINC OXIDE	Crown Laboratories	3368f1cb-c341-e886-e063-6394a90a9b7c	2026-01-12	Warnings	Exact identifier application number: M020
Blue Lizard Sport SPF 50 Sunscreen	TITANIUM DIOXIDE AND ZINC OXIDE	Crown Laboratories	2f3844d8-0367-aad9-e063-6294a90a1fce	2026-01-12	Warnings	Exact identifier application number: M020
Blue Lizard Sheer Face SPF 50 Sunscreen	TITANIUM DIOXIDE AND ZINC OXIDE	Crown Laboratories	30cd79da-2f25-a42a-e063-6394a90a8332	2026-01-12	Warnings	Exact identifier application number: M020
ACCOJE PROTECTIVE AIR-FIT MINERAL SUNSCREEN	TITAMIUN DIOXIDE, ZINC OXIDE	UCL Co., Ltd.	4837b4f6-ada9-801a-e063-6294a90a8547	2026-01-12	Warnings	Exact identifier application number: M020
Intellishade Original SPF 45	OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE	Revision, LLC	e213a681-eb22-69c0-e053-2995a90a899e	2026-01-12	Warnings	Exact identifier application number: M020
GINZING SPF 40 ENERGY-BOOSTING TINTED MOISTURIZER BROAD SPECTRUM SPF 40 SHEER TINT RELEASE	HOMOSALATE,OCTINOXATE,OCTISALATE, AND ZINC OXIDE	ORIGINS NATURAL RESOURCES INC.	48393640-4b97-04de-e063-6294a90aa6a6	2026-01-12	Warnings	Exact identifier application number: M020
Hale and Hush Broad Spectrum SPF 30 SPF 30	ZINC OXIDE	Eclectic Solutions LLC	0530904f-b02c-d8cf-e063-6294a90aa5a7	2026-01-12	Warnings	Exact identifier application number: M020
Minori Daily Mineral Face Sunscreen Broad Spectrum SPF 30	ZINC OXIDE	Minori Inc.	1d4e2654-1638-0d01-e063-6394a90af303	2026-01-12	Warnings	Exact identifier application number: M020
LUXURY BODY RITUAL HYDRATING SPF 30	ZINC OXIDE	JANE STREET LLC	15e9d688-f226-1a19-e063-6394a90ab906	2026-01-12	Warnings	Exact identifier application number: M020
BROAD SPECTRUM SPF50 SPF 50	AVOBENZONE, HOMOSALATE OCTISALATE,	NAKED SUNDAYS PTY LTD	0426b1e9-063b-c1e6-e063-6294a90a2554	2026-01-11	Warnings	Exact identifier application number: M020
SPF30 MINERAL SUNSCREEN MOUSSE	ZINC OXIDE	Aopline Biotechnology (Guangzhou) Co., Ltd.	48031a0f-c2ed-5424-e063-6294a90ad0ff	2026-01-10	Warnings	Exact identifier application number: M020
SPF 30 MINERAL WHIPPED CREAMS SHIMMER	ZINC OXIDE	Aopline Biotechnology (Guangzhou) Co., Ltd.	48037a05-722e-4231-e063-6294a90ac51f	2026-01-10	Warnings	Exact identifier application number: M020
ODLUMIVIE Tinted Mineral Sunscreen	ZINC OXIDE,TITANIUM DIOXIDE	Guangzhou Meijiao Medical Biotechnology Co., Ltd.	480d6e65-f6dc-d2a5-e063-6294a90a24a1	2026-01-10	Warnings	Exact identifier application number: M020
Cloud Brush On Sunscreen Clear Broad Spectrum SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	FUTURE 8 LLC	9922f132-f6a5-41ca-847a-936b20bf1716	2026-01-09	Warnings	Exact identifier application number: M020
Sunscreen Lotion118mL	ZINC OXIDE 15%, TITANIUM DIOXIDE 6%, HOMOSALATE 5%, OCTISALATE 4%	Foshan Sugar Max Cosmetics CO.,Ltd	46355437-4068-9d03-e063-6394a90ae52c	2026-01-09	Warnings	Exact identifier application number: M020
ST MORIZ SUNCARE FACE SUNSCREEN SPF30	SUNCARE FACE SUNSCREEN SPF30	Aopline Biotechnology (Guangzhou) Co., Ltd.	47f26af6-4d02-3506-e063-6294a90a0fe6	2026-01-09	Warnings	Exact identifier application number: M020
Dr. C. Tuna Sun 6 SPF Tan and Care Carrot	OCTINOXATE	Farmasi US LLC	67de9257-70f3-4444-a4a2-a8d7425fcc0e	2026-01-09	Warnings	Exact identifier application number: M020
Dr. C. Tuna Sunscreen SPF30 Broad Spectrum	AVOBENZONE, OCTINOXATE, OCTOCRYLENE, HOMOSALATE	Farmasi US LLC	d9197dce-20a3-4d10-807c-ec84ab902165	2026-01-09	Warnings	Exact identifier application number: M020
Dr. C. Tuna Lumi Radiance Brightening	OCTOCRYLENE, OCTINOXATE, AVOBENZONE	Farmasi US LLC	adf5621b-7cf0-53b3-e053-2a95a90a8058	2026-01-09	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