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		2026-10-12

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 2 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Intense Therapy Lip Balm Asian Pear	SUNSCREEN SKIN PROTECTANT LIP BALM	Jack Black, LLC	acace707-6671-4818-86f2-d9813792157a	2026-09-08	Warnings	Exact identifier application number: M020
Intense Therapy Lip Balm Basil Lemon	SUNSCREEN SKIN PROTECTANT LIP BALM	Jack Black, LLC	277cb44d-608a-4ffc-a2a5-ac57d33d214c	2026-09-08	Warnings	Exact identifier application number: M020
Intense Therapy Lip Balm Black Cherry	SUNSCREEN SKIN PROTECTANT LIP BALM	Jack Black, LLC	8f413bd6-258c-4c3c-89d1-369938c85720	2026-09-08	Warnings	Exact identifier application number: M020
Intense Therapy Lip Balm Cucumber Lime	SUNSCREEN SKIN PROTECTANT LIP BALM	Jack Black, LLC	5f15bee9-9bf4-4f27-a6b5-4205deb625f6	2026-09-08	Warnings	Exact identifier application number: M020
Intense Therapy Lip Balm Winter Melon	SUNSCREEN SKIN PROTECTANT LIP BALM	Jack Black, LLC	e7792b4e-a6d2-487e-ba28-27b68e6d7e27	2026-09-08	Warnings	Exact identifier application number: M020
Jack Black Intense Therapy Lip Balm Vanilla Bourbon	AVOBENZONE, OCTINOXATE LIP BALM SUNSCREEN	Jack Black, LLC	517040d1-e6ed-40ca-a46f-2f75403dbc3c	2026-09-08	Warnings	Exact identifier application number: M020
Intense Therapy Lip Balm Mango and Mandarin	SUNSCREEN SKIN PROTECTANT LIP BALM	Jack Black, LLC	8c55d1cd-cdd6-468b-8a17-b940c6210116	2026-09-08	Warnings	Exact identifier application number: M020
Jack Black Intensive Therapy Lip Balm Mango Chili Lime	AVOBENZONE, OCTINOXATE LIP BALM SUNSCREEN	Jack Black, LLC	51349d57-b14d-4798-8d68-03fbe3713d1e	2026-09-08	Warnings	Exact identifier application number: M020
Jack Black Sun Guard Sunscreen SPF45	SUNSCREEN	Jack Black, LLC	3cc86bb2-05ce-47eb-8c71-f4f116ca5840	2026-09-08	Warnings	Exact identifier application number: M020
Jack Black Intense Thearpy Lip Balm SPF25, Lemon and Shea Butter	LIP BALM SUNSCREEN	Jack Black, LLC	518cb17a-fdaa-4a60-93fc-708305366eb8	2026-09-08	Warnings	Exact identifier application number: M020
Jack Black Lavender Lip Balm 0.25oz	LIP BALM SUNSCREEN	Jack Black, L.L.C.	e8c6a6d9-1093-41f1-87d5-faf8583d4319	2026-09-08	Warnings	Exact identifier application number: M020
SPF15 lip balm 01	OCTOCRYLENE, OCTISALATE	Cosmuses Cosmetics (Ningbo) Co., Ltd.	f8695305-b89d-c21c-e053-6394a90a0e84	2026-09-08	Warnings	Exact identifier application number: M020
Sunscreen stick	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Cosmuses Cosmetics (Ningbo) Co., Ltd.	e9f963ee-a98c-efc1-e053-2a95a90aaf53	2026-09-08	Warnings	Exact identifier application number: M020
SPF30 Sunscreen 01	AVOBENZONE ,HOMOSALATE,OCTOCRYLENE, OCTISALATE	Cosmuses Cosmetics (Ningbo) Co., Ltd.	5b04751d-32e9-a7e2-e063-6294a90aefbd	2026-09-08	Warnings	Exact identifier application number: M020
Juyasuyon Invisible Sunscreen	HOMOSALATE,OCTOCRYLENE,OCTISALATE,BEMOTRIZINOL,AVOBENZONE	Guangdong Aimu Biological Technology Co., Ltd	5ab335b5-bb9e-4642-e063-6294a90a3986	2026-09-05	Warnings	Exact identifier application number: M020
No7 Future Renew Defense Shield SPF 50	AVOBENZONE, OCTINOXATE, OCTISALATE	BCMC	41cc2c52-c6a4-611c-e063-6294a90aae01	2026-09-03	Warnings	Exact identifier application number: M020
WALMART EQUATE SUNSCREEN SPF 50 SPORT BROAD SPECTRUM	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	WALMART, INC.	58b5d0ce-9157-9dee-e063-6394a90ab543	2026-09-02	Warnings	Exact identifier application number: M020
Chantecaille Ultra Sun Protection Sunscreen SPF 45	AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE	Chantecaille Beaute Inc	6186ea56-7d56-43f5-985d-a012f1296afa	2026-09-02	Warnings	Exact identifier application number: M020
ULTRA VIOLETTE Fave Screen Broad Spectrum SPF 50	AVOBENZONE, BEMOTRIZINOL, OCTISALATE	Grace and Fire USA	5739c5b9-00d8-75a8-e063-6394a90aa8c7	2026-09-01	Warnings	Exact identifier application number: M020
Sun Wave Anti Aging Insta Dry SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Sun Life Brands, LLC	2d5fa597-08a8-41ca-ba9e-b52e41a5c70c	2026-09-01	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