Everyday Facial Moisturizer And Sunscreen SPF 20

Product NDC: 76230-727
11-digit product format: 762300727
Labeler code: 76230
Product ID: 76230-727_0c5baaf8-ed77-5c24-e063-6394a90a9f3c
Type: HUMAN OTC DRUG
Nonproprietary name: ZINC OXIDE
Dosage form: CREAM
Route: TOPICAL
Labeler: 714 Essentials LTD
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2011-06-09
Substance: ZINC OXIDE
Active strength: 163.2 mg/mL
NDC exclude flag: No
Listing certified through: 2027-12-31
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 · 18 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 product	product		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	76230-727-09	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	76230-727-09	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
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	76230-727-09	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	76230-727-09	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	76230-727-09	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	76230-727-09	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	76230-727-09	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	76230-727-09	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	76230-727-09	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: Everyday Facial Moisturizer And Sunscreen SPF 20
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ZINC OXIDE	163.2 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
SOI2LOH54Z	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
3a29018b-8103-4983-b0c5-5f340775a05d	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76230-727-09	2026-01-23	C162847	48780-1	2cef2736-9f49-d83d-e063-dadaa90ab31f	Everyday Facial Moisturizer And Sunscreen SPF 20
76230-727-09	2025-01-30	C162847	48780-1	2cef2736-9f49-d83d-e063-dadaa90ab31f	Everyday Facial Moisturizer And Sunscreen SPF 20

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76230-727-09	Everyday Facial Moisturizer And Sunscreen SPF 20	75 mL in 1 BOTTLE	CREAM	75		7
76230-727-09	Everyday Facial Moisturizer And Sunscreen SPF 20	1 in 1 PACKAGE	CREAM	1		7

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ZINC OXIDE	ACTIVE INGREDIENT	SOI2LOH54Z	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	1
ZINC OXIDE	ACTIVE MOIETY	SOI2LOH54Z	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	1
BUTYLENE GLYCOL	INACTIVE INGREDIENT	3XUS85K0RA	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	1
CAPRYLYL GLYCOL	INACTIVE INGREDIENT	00YIU5438U	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	1
CHLORPHENESIN	INACTIVE INGREDIENT	I670DAL4SZ	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	1
CYCLOMETHICONE 5	INACTIVE INGREDIENT	0THT5PCI0R	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	1
DIMETHICONE	INACTIVE INGREDIENT	92RU3N3Y1O	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	1
DIPROPYLENE GLYCOL	INACTIVE INGREDIENT	E107L85C40	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	1
EDETATE DISODIUM	INACTIVE INGREDIENT	7FLD91C86K	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	1
GLYCYRRHIZINATE DIPOTASSIUM	INACTIVE INGREDIENT	CA2Y0FE3FX	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	1
GREEN TEA LEAF	INACTIVE INGREDIENT	W2ZU1RY8B0	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	1
HYALURONATE SODIUM	INACTIVE INGREDIENT	YSE9PPT4TH	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	1
ISONONYL ISONONANOATE	INACTIVE INGREDIENT	S4V5BS6GCX	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	1
PANTHENOL	INACTIVE INGREDIENT	WV9CM0O67Z	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	1
PHENOXYETHANOL	INACTIVE INGREDIENT	HIE492ZZ3T	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	1
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	1
SODIUM PYRROLIDONE CARBOXYLATE	INACTIVE INGREDIENT	469OTG57A2	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76230-727	EVERYDAY FACIAL MOISTURIZER AND SUNSCREEN SPF 20 (ZINC OXIDE) CREAM [714 ESSENTIALS LTD]	6	Current NDC, Legacy NDC, 2 package rows	20230221_3a29018b-8103-4983-b0c5-5f340775a05d.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 129 of 353 · 7,049 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Join
Canopy SPF 40 Tinted	ZINC OXIDE	BORREGO SPRINGS SKINCARE LLC	358319c5-ae35-cb3b-e063-6394a90ad77f	2025-12-12	Exact identifier application number: M020
Non-Tinted Matte Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Skin Philosophy by Kelly	3581ab49-ef55-3743-e063-6394a90a3bd5	2025-12-12	Exact identifier application number: M020
Matte Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Skin Philosophy by Kelly	3581cf33-3520-42f7-e063-6394a90a6f93	2025-12-12	Exact identifier application number: M020
Mineral Sunscreen For Face and Body	ZINC OXIDE	Skin Philosophy by Kelly	358248e6-16cf-6f9b-e063-6394a90a55d7	2025-12-12	Exact identifier application number: M020
Replenishing Mineral Sunscreen	ZINC OXIDE	Skin Philosophy by Kelly	35828e76-66db-49de-e063-6294a90a2b99	2025-12-12	Exact identifier application number: M020
Matte Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Skin Philosophy by Kelly	3592b2c7-295a-7c60-e063-6394a90a387b	2025-12-12	Exact identifier application number: M020
Mineral Sunscreen For Face and Body	ZINC OXIDE	Skin Philosophy by Kelly	3592fd5f-13d1-9aec-e063-6394a90abd67	2025-12-12	Exact identifier application number: M020
Replenishing Mineral Sunscreen	ZINC OXIDE	Skin Philosophy by Kelly	359371f2-2407-e1a1-e063-6294a90a2165	2025-12-12	Exact identifier application number: M020
Non Tinted Sheer Mineral Zinc Sunscreen	ZINC OXIDE	SKIN THERAPY PLLC	397fc3c9-9d30-adcf-e063-6394a90ac761	2025-12-12	Exact identifier application number: M020
Non Tinted Sheer Mineral Zinc Sunscreen	ZINC OXIDE	SKIN THERAPY PLLC	39800bf1-e01a-e1c8-e063-6294a90a53bf	2025-12-12	Exact identifier application number: M020
Tinted Sheer Mineral Zinc Sunscreen	ZINC OXIDE	SKIN THERAPY PLLC	397130ea-dfad-ecd3-e063-6394a90a7da4	2025-12-12	Exact identifier application number: M020
Tinted Sheer Mineral Zinc Sunscreen	ZINC OXIDE	SKIN THERAPY PLLC	39716532-a699-63b7-e063-6294a90aa0f0	2025-12-12	Exact identifier application number: M020
Sun Elegant Mineral Sunscreen Tinted	TITANIUM DIOXIDE, ZINC OXIDE	SKIN BY NESRIN	3580ae10-1867-cb68-e063-6394a90a72df	2025-12-12	Exact identifier application number: M020
Simply Zinc Mineral Sunscreen Tinted	ZINC OXIDE	SKIN BY NESRIN	3580da4f-116d-8108-e063-6294a90a7bf4	2025-12-12	Exact identifier application number: M020
PROTECTOR SOLAR NON-TINTED SPF SUNSCREEN	TITANIUM DIOXIDE, ZINC OXIDE	The Beez Kneez Skin Care & Acne Clinic LLC	358195c0-6d28-1ffe-e063-6394a90a6027	2025-12-12	Exact identifier application number: M020
PROTECTOR SOLAR TINTED SPF SUNSCREEN	ZINC OXIDE	The Beez Kneez Skin Care & Acne Clinic LLC	3581d973-ac0b-7d2e-e063-6294a90ae2b3	2025-12-12	Exact identifier application number: M020
Matte Velvet Tint	TITANIUM DIOXIDE, ZINC OXIDE	Brent Loftis, D.O., Inc., A California Medical Corporation	3583f860-664b-2658-e063-6394a90a3857	2025-12-12	Exact identifier application number: M020
Satin Tint	ZINC OXIDE	Brent Loftis, D.O., Inc., A California Medical Corporation	35920108-7f8a-27d4-e063-6294a90a0ef6	2025-12-12	Exact identifier application number: M020
SPF Lip	TITANIUM DIOXIDE, ZINC OXIDE	Brent Loftis, D.O., Inc., A California Medical Corporation	359297cd-10e2-6ddd-e063-6394a90a4aa0	2025-12-12	Exact identifier application number: M020
Matte Velvet Tint	TITANIUM DIOXIDE, ZINC OXIDE	Brent Loftis, D.O., Inc., A California Medical Corporation	359641c5-0e19-f243-e063-6394a90aeebc	2025-12-12	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
SOI2LOH54Z	ZINC OXIDE	1314-13-2	ZINC OXIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
76230-727-09	76230072709	1 BOTTLE in 1 PACKAGE (76230-727-09) / 75 mL in 1 BOTTLE	1 bottle	2017-12-19	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Everyday Facial Moisturizer And Sunscreen SPF 20	714 Essentials LTD \| Englewood Lab, Inc.	2023-12-12	HUMAN OTC DRUG LABEL	7