DAILY FACE SUNSCREEN

Product NDC: 81781-101
11-digit product format: 817810101
Labeler code: 81781
Product ID: 81781-101_4cea6540-71eb-1476-e063-6394a90ab19c
Type: HUMAN OTC DRUG
Nonproprietary name: Zinc Oxide
Dosage form: CREAM
Route: TOPICAL
Labeler: Lilyana Naturals LLC
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-07-15
Substance: ZINC OXIDE
Active strength: 10 g/100g
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	81781-101-50	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	81781-101-50	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	81781-101-50	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	81781-101-50	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	81781-101-50	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	81781-101-50	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	81781-101-50	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	81781-101-50	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	81781-101-50	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: DAILY FACE SUNSCREEN
Brand name suffix: Broad Spectrum SPF 30
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ZINC OXIDE	10 g/100g

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
e5f53e2f-6566-4eac-b9b5-7697abaf044b	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
81781-101-50	2025-01-30	C162847	48780-1	2cef2736-af93-d83d-e063-dadaa90ab31f	DAILY FACE Zinc Oxide Sunscreen BROAD SPECTRUM SPF 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
81781-101-50	DAILY FACE SUNSCREENBroad Spectrum SPF 30	1 in 1 CARTON	CREAM	1		2
81781-101-50	DAILY FACE SUNSCREENBroad Spectrum SPF 30	48 g in 1 TUBE	CREAM	48		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81781-101	DAILY FACE SUNSCREEN BROAD SPECTRUM SPF 30 (ZINC OXIDE) CREAM [LILYANA NATURALS LLC]	1	Current NDC, Legacy NDC, 2 package rows	20210722_e5f53e2f-6566-4eac-b9b5-7697abaf044b.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 133 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Join
Tinted Mineral Matte CE Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	The Maui Medical Group, Inc	34b72d14-b69b-e9dd-e063-6394a90a748e	2025-12-11	Exact identifier application number: M020
Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	SCIENCE CEUTICALS, LLC	369b20e2-2cad-e047-e063-6294a90a1bba	2025-12-11	Exact identifier application number: M020
Tinted Mineral Matte CE Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	The Maui Medical Group, Inc	34b60880-5fe1-b78f-e063-6294a90a748d	2025-12-11	Exact identifier application number: M020
Sheer Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	The Maui Medical Group, Inc	34b51190-6a6d-c5e0-e063-6394a90ae875	2025-12-11	Exact identifier application number: M020
Tinted Ultra Zinc Face and Body	ZINC OXIDE	LIV BODY AND BEAUTY LLC	374fae34-41b9-4cab-e063-6394a90a9b1d	2025-12-11	Exact identifier application number: M020
Z Bloc	ZINC OXIDE	The Maui Medical Group, Inc	34b64eb5-a91f-de43-e063-6294a90a8043	2025-12-11	Exact identifier application number: M020
Sheer Tinted Sunscreen Stick	TITANIUM DIOXIDE, ZINC OXIDE	The Maui Medical Group, Inc	34b6e8d0-6235-dac2-e063-6394a90afefd	2025-12-11	Exact identifier application number: M020
Tinted Sunscreen Face Primer	TITANIUM DIOXIDE, ZINC OXIDE	LIV BODY AND BEAUTY	374f6b79-2ac4-61cf-e063-6394a90a699b	2025-12-11	Exact identifier application number: M020
Non Tinted Ultra Zinc Face and Body	ZINC OXIDE	LIV BODY AND BEAUTY LLC	375008f2-8dd4-aa31-e063-6394a90a5be8	2025-12-11	Exact identifier application number: M020
Replenishing Daily Protection	ZINC OXIDE	The Maui Medical Group, Inc	34b96d82-7fcf-e452-e063-6394a90a781b	2025-12-11	Exact identifier application number: M020
Daily Sun Defense	TITANIUM DIOXIDE, ZINC OXIDE	LIV BODY AND BEAUTY LLC	3750c2fd-c5cc-fd00-e063-6394a90aeb89	2025-12-11	Exact identifier application number: M020
Non Tinted Ultra Zinc Face and Body	ZINC OXIDE	LIV BODY AND BEAUTY LLC	3750ffbf-a82d-b4b9-e063-6294a90a7d68	2025-12-11	Exact identifier application number: M020
The Block	ZINC OXIDE	ELITE ESTHETICS BY NICOLE CAROLINE LLC	34a6b17e-6e9e-3f2c-e063-6294a90a1c32	2025-12-11	Exact identifier application number: M020
SPF 40 Broad Spectrum Non-Tinted	ZINC OXIDE	Teton Dermatology Holdings, Inc.	35093797-008b-b265-e063-6294a90a9949	2025-12-11	Exact identifier application number: M020
Tinted Zinc Protection	ZINC OXIDE	Teton Dermatology Holdings, Inc.	3508d5a8-9d3c-51d1-e063-6394a90abc8e	2025-12-11	Exact identifier application number: M020
SPF 40 Broad Spectrum	TITANIUM DIOXIDE, ZINC OXIDE	Teton Dermatology Holdings, Inc.	35081ce0-2203-ab86-e063-6294a90aefd5	2025-12-11	Exact identifier application number: M020
Antioxidant SPF	ZINC OXIDE	Teton Dermatology Holdings, Inc.	3509a916-f3e1-9c53-e063-6394a90a5bff	2025-12-11	Exact identifier application number: M020
Ultimate Physical Sunscreen Tinted	ZINC OXIDE	HALEM DERMATOLOGY PLLC	35bb4953-ca8c-e927-e063-6394a90a1a31	2025-12-11	Exact identifier application number: M020
Lip Protection	TITANIUM DIOXIDE, ZINC OXIDE	Teton Dermatology Holdings, Inc.	3509eea7-f966-2080-e063-6294a90aeeb5	2025-12-11	Exact identifier application number: M020
Mineral Lip Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	HALEM DERMATOLOGY PLLC	35bce44e-d9f4-9279-e063-6394a90a6453	2025-12-11	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
81781-101-50	81781010150	1 TUBE in 1 CARTON (81781-101-50) / 48 g in 1 TUBE	1 tube	2021-07-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
DAILY FACE Zinc Oxide Sunscreen BROAD SPECTRUM SPF 30	Lilyana Naturals LLC \| Atlantis Laboratories, Inc.	2026-03-13	HUMAN OTC DRUG LABEL	2