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 164 of 354 · 7,077 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SOME BY MI V10 HYAL AIR FIT SUNSCREEN	SUNSCREENT	PERENNEBELL	fe2148db-9020-9343-e053-6294a90adf70	2025-11-13	Warnings	Exact identifier application number: M020
skin MD	OCTINOXATE, OCTISALATE, HOMOSALATE	21st Century Formulations	e809e1d3-0a6d-730d-e053-2a95a90aedb9	2025-11-13	Warnings	Exact identifier application number: M020
Obagi Nu-Derm Fx System Normal-Oily Skin Transformation Complexion Brightening System	TITANIUM DIOXIDE, ZINC OXIDE	Obagi Cosmeceuticals LLC	a64045dd-8f70-43f1-be6f-ad1556c0e210	2025-11-13	Warnings	Exact identifier application number: M020
Florida Glow SPF 50	AVOBENZONE,OCTOCRYLENE,OCTISALATE,HOMOSALATE	Southeast Holdings Corp.	dcb43ee0-5ab0-495a-8e68-90cab881337d	2025-11-12	Warnings	Exact identifier application number: M020
Florida Glow SPF 30	AVOBENZONE,OCTOCRYLENE,OCTISALATE,HOMOSALATE	Southeast Holdings Corp.	20538bc0-10c3-492c-952a-6797e46003f2	2025-11-12	Warnings	Exact identifier application number: M020
Florida Glow SPF 15	AVOBENZONE,OCTOCRYLENE,OCTISALATE	Southeast Holdings Corp.	56af704a-bda9-49ed-a177-a8480d90458b	2025-11-12	Warnings	Exact identifier application number: M020
Florida Glow face shield SPF 55	HOMOSALATE, OCTOCRYLENE, ZINC OXIDE	Southeast Holdings Corp.	cea54600-5308-4b9f-98ca-fef0b26d79c1	2025-11-12	Warnings	Exact identifier application number: M020
Florida Glow SPF 30	ZINC OXIDE	Southeast Holdings Corp.	4bf1ca6b-5d87-40ee-97f4-89f1bfadcecb	2025-11-12	Warnings	Exact identifier application number: M020
TuroSkin Daily Moisturizing Sunscreen broadspectrum spf15	AVOBENZONE,HOMOSALATE,OCTISALATE	Renuskin LLC	e36efd74-11c2-4850-9529-1c88b7364a33	2025-11-12	Warnings	Exact identifier application number: M020
TuroSkin Sport Sunscreen Broad Spectrum SPF 30 WR SR 80min	AVOBENZONE,HOMOSALATE,OCTISALATE	Renuskin LLC	22a40d93-ca67-4b7d-a95c-22f52cd6d297	2025-11-12	Warnings	Exact identifier application number: M020
ZEUS	ZINC OXIDE	NEWPORT APOTHECARY, INC	5354c383-08f0-4b89-b36a-96a35f47be3c	2025-11-12	Warnings	Exact identifier application number: M020
Practical Alchemy Hydrating SPF 30	ZINC OXIDE	Over Here, LLC	2f07df5b-dbd4-494c-a7cf-55843fb4d7c2	2025-11-12	Warnings	Exact identifier application number: M020
Dr Lift SPF 50 Mineral Sunscreen Stick	ZINC OXIDE	Spa de Soleil	436fdf4f-11db-7c5b-e063-6294a90a8731	2025-11-12	Warnings	Exact identifier application number: M020
CeraVe Developed with Dermatologists Skin Renewing Brightening with Sunscreen Broad Spectrum SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	L'Oreal USA Products Inc	3676aa91-c90d-4a7a-b02e-d5b35304a04d	2025-11-12	Warnings	Exact identifier application number: M020
HYDRATING GLOW MIST SPF 50	AVOBENZONE, OCTISALATE, OCTOCRYLENE	NAKED SUNDAYS PTY LTD	df3bd18d-63b4-460f-bf1c-115ad35edd96	2025-11-11	Warnings	Exact identifier application number: M020
Zinka Clear Zinc Oxide Sunscreen	OCTINOXATE, ZINC OXIDE, OCTISALATE, OXYBENZONE	Zinka, Inc.	7b097f5e-8127-49e6-8a77-4ee1fded5ff1	2025-11-11	Warnings	Exact identifier application number: M020
Total Sun Protection	OCTINOXATE, OCTISALATE, OXYBENZONE, ZINC OXIDE	Cosmed Dermaceuticals, Inc.	dbb16ef1-ab8c-4e71-a2a2-a507d104ff0f	2025-11-11	Warnings	Exact identifier application number: M020
Sunsorb Reef Safe SPF15	HOMOSALATE, OCTOCRYLENE, AVOBENZONE	QS Key West Aloe, LLC	1a1c17c4-4912-4573-9f59-cbd14a014cb4	2025-11-11	Warnings	Exact identifier application number: M020
Sunsorb Reef Safe SPF30	HOMOSALATE, OCTOCRYLENE, AVOBENZONE	QS Key West Aloe, LLC	14f65b3d-90bf-4689-aa6e-879e06153db9	2025-11-11	Warnings	Exact identifier application number: M020
Sunsorb Reef Safe SPF50	HOMOSALATE, ZINC OXIDE, OCTOCRYLENE	QS Key West Aloe, LLC	b4fc7a51-a163-4057-8790-f2111668ec67	2025-11-11	Warnings	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