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 143 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Tinted Mineral Sunscreen 20% Zinc Oxide	ZINC OXIDE	INTEGRATIVE AESTHETICS BOSTON, LLC	31416d04-2d6f-7cf9-e063-6294a90a9806	2025-12-09	Warnings	Exact identifier application number: M020
Matte Invisible Mineral Sunscreen Non-Tinted	ZINC OXIDE	INTEGRATIVE AESTHETICS BOSTON, LLC	3143968a-096e-b9ac-e063-6294a90ada0d	2025-12-09	Warnings	Exact identifier application number: M020
Daily Mineral Sunscreen 20% Zinc Oxide	ZINC OXIDE	INTEGRATIVE AESTHETICS BOSTON, LLC	314299b1-a78b-c1bd-e063-6294a90ab43b	2025-12-09	Warnings	Exact identifier application number: M020
Sheer Satin Mineral Sunscreen Tinted	TITANIUM DIOXIDE, ZINC OXIDE	INTEGRATIVE AESTHETICS BOSTON, LLC	3143d8b0-4af8-f52d-e063-6294a90a926b	2025-12-09	Warnings	Exact identifier application number: M020
Matte Invisible Mineral Sunscreen	ZINC OXIDE	INTEGRATIVE AESTHETICS BOSTON, LLC	3142ed0f-f379-f240-e063-6294a90a5303	2025-12-09	Warnings	Exact identifier application number: M020
Sheer Non-Tinted Mineral Sunscreen Stick	TITANIUM DIOXIDE, ZINC OXIDE	Face Collection, L.L.C.	33d83cfb-045d-141c-e063-6394a90a2e04	2025-12-09		Exact identifier application number: M020
First Aid Beauty FAB Ultra Light Mineral Sunscreen Broad Spectrum SPF 30	ZINC OXIDE	The Procter & Gamble Manufacturing Company	45875865-5e9c-d652-e063-6394a90ad5fa	2025-12-09	Warnings	Exact identifier application number: M020
Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Maloney Plastic Surgery Skin Care, PLLC	316b7584-c782-fe9e-e063-6394a90a76fe	2025-12-09		Exact identifier application number: M020
Transparent Tinted Mineral Sunscreen Stick	TITANIUM DIOXIDE, ZINC OXIDE	Face Collection, L.L.C.	33dbfd9b-b90f-bb32-e063-6294a90af7dc	2025-12-09		Exact identifier application number: M020
Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Maloney Plastic Surgery Skin Care, PLLC	316b46ac-6dde-72d1-e063-6294a90a03da	2025-12-09		Exact identifier application number: M020
Replenish	ZINC OXIDE	Maloney Plastic Surgery Skin Care, PLLC	316c43fb-0c15-87d4-e063-6294a90a0a63	2025-12-09		Exact identifier application number: M020
BIOJUVE Microbiome-Safe Sheer Finish SPF 50 Sunscreen	TITANIUM DIOXIDE AND ZINC OXIDE	Crown Laboratories	ece7565b-f3e5-3386-e053-2a95a90a5802	2025-12-09	Warnings	Exact identifier application number: M020
Hydraboost Lip Treatment	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Bluemercury	2cf30083-8723-23f6-e063-6394a90a55de	2025-12-09	Warnings	Exact identifier application number: M020
Florida Babe Sport Non-Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Tichy Anesthesia PA	31e4756d-8604-6e75-e063-6294a90aebe1	2025-12-09		Exact identifier application number: M020
Florida Babe Sport Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Tichy Anesthesia PA	31e4d9ae-f532-f9f5-e063-6294a90a8d39	2025-12-09		Exact identifier application number: M020
Arbonne FunSun Mineral Sunscreen Broad Spectrum SPF 30	ZINC OXIDE	Arbonne International, LLC	91bcd120-28e5-4f44-9522-550c1dbcd82c	2025-12-09	Warnings	Exact identifier application number: M020
Florida Babe Active Tinted 20percent Zinc Oxide Mineral Sunscreen	ZINC OXIDE	Tichy Anesthesia PA	31e509f2-dcb6-5ae0-e063-6394a90a70c1	2025-12-09		Exact identifier application number: M020
Florida Babe Active Non-Tinted 20percent Zinc Oxide Mineral Sunscreen	ZINC OXIDE	Tichy Anesthesia PA	31e57817-b8c4-8178-e063-6294a90a0149	2025-12-09		Exact identifier application number: M020
Florida Babe Everyday Tinted Replenishing Daily Protection	ZINC OXIDE	Tichy Anesthesia PA	3231f1fe-51b3-b2e7-e063-6394a90a2758	2025-12-09		Exact identifier application number: M020
Florida Babe Everyday Tinted Replenishing Daily Protection	ZINC OXIDE	Tichy Anesthesia PA	31e63876-3e39-adc6-e063-6394a90ab146	2025-12-09		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