Kiss My Face Purely Mineral Daily 50 Sunscreen SPF 50

Product NDC: 74154-903
11-digit product format: 741540903
Labeler code: 74154
Product ID: 74154-903_4ba3d83b-0005-b5de-e063-6294a90acc39
Type: HUMAN OTC DRUG
Nonproprietary name: ZINC OXIDE
Dosage form: LOTION
Route: TOPICAL
Labeler: Windmill Health Products, LLC
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2026-02-04
Substance: ZINC OXIDE
Active strength: 175 mg/mL
Pharmacologic classes: Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

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: Kiss My Face Purely Mineral Daily 50 Sunscreen SPF 50
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ZINC OXIDE	175 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
ebfb149c-0371-4492-b03a-5fdcb7821753	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74154-903-00	Kiss My Face Purely Mineral Daily 50 Sunscreen SPF 50	118 mL in 1 BOTTLE	LOTION	118		1

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 282 of 346 · 6,912 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
H.E.B Solutions Sunscreen	SPORT SPF 70 CONTINUOUS SPRAY	H.E.B	f9b5b360-6b69-4006-934f-5bc8a9fdfcd0	2024-10-15	Warnings	Exact identifier application number: M020
HEB	GENERAL PROTECTION SPF 100 LOTION	H-E-B	39d94e3a-98c8-44b0-bd2d-f318ac7bbf75	2024-10-15	Warnings	Exact identifier application number: M020
H.E.B Solutions Sunscreen	WET PROTECTION KIDS SPF 70 CONTINUOUS SPRAY	H.E.B	f823b236-5884-41d9-bff0-65b91664aaad	2024-10-15	Warnings	Exact identifier application number: M020
H.E.B Solutions Sunscreen	COOLING SPORT SPF 50 CONTINUOUS SPRAY	H.E.B	67fdf3a0-08fe-4348-a4f9-a83f3cf46b72	2024-10-15	Warnings	Exact identifier application number: M020
H.E.B Solutions Sunscreen	ULTRA SPF 70 CONTINUOUS SPRAY	H.E.B	c16935ce-afdb-4571-b5a3-6dc5d01f721c	2024-10-15	Warnings	Exact identifier application number: M020
H.E.B Solutions Sunscreen	BABY SPF 50 LOTION SPRAY	H.E.B	1082111f-bf04-4a98-b6a0-5da933652f1d	2024-10-15	Warnings	Exact identifier application number: M020
H.E.B ULTRA	SPF 50 SUNSCREEN	H.E.B	d6184ba2-0e47-459a-8777-1f27be2140a6	2024-10-15	Warnings	Exact identifier application number: M020
H.E.B ULTRA	SPF 30 SUNSCREEN	H.E.B	90287874-cdfa-489c-936d-e487f6b3db96	2024-10-15	Warnings	Exact identifier application number: M020
H.E.B	SPF 50 SUNSCREEN	H.E.B	2c9258ac-8cbe-4acf-9c02-bb993d69a3e5	2024-10-15	Warnings	Exact identifier application number: M020
H.E.B	SPF 50 SUNSCREEN	H.E.B	39bf1379-3dee-4aa0-967a-36faccca4216	2024-10-15	Warnings	Exact identifier application number: M020
H.E.B Solutions Sunscreen	SPORT SPF 100 CONTINUOUS SPRAY	H.E.B	301ae7e5-5a60-45d0-8cd5-553ba07db4c5	2024-10-15	Warnings	Exact identifier application number: M020
Positive Light Tinted Moisturizer Broad Spectrum SPF 20 Sunscreen 28C	HOMOSALATE, ZINC OXIDE	Rare Beauty, LLC	2470d78c-724f-4181-e063-6294a90afeaa	2024-10-14	Warnings	Exact identifier application number: M020
Positive Light Tinted Moisturizer Broad Spectrum SPF 20 Sunscreen 44N	HOMOSALATE, ZINC OXIDE	Rare Beauty, LLC	2471e0fa-ddc8-1c62-e063-6294a90a4408	2024-10-14	Warnings	Exact identifier application number: M020
Walgreens 70 Hydrating Sport Broad Spectrum SPF 70 Sunscreen	AVOBENZONE. HOMOSALATE, OCTISALATE, OCTOCRYLENE	WALGREEN COMPANY	fa2d08be-f67f-60dd-e053-6294a90adb3f	2024-10-14	Warnings	Exact identifier application number: M020
Walgreens 90 Sport Continuous	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	WALGREEN COMPANY	fa2e5b1b-f38f-11fe-e053-6394a90a4988	2024-10-14	Warnings	Exact identifier application number: M020
Walgreens 70 Sheer Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	WALGREEN COMPANY	fc635082-0a7a-f160-e053-6394a90abba3	2024-10-14	Warnings	Exact identifier application number: M020
WALGREENS SPORT SPF 50 SUNSCREEN	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Walgreen Company	a9ee1c60-6091-2229-e053-2995a90aa528	2024-10-14	Warnings	Exact identifier application number: M020
WALGREENS BROAD SPECTRUM SPORT SPF 50 SUNSCREEN	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	WALGREEN COMPANY	b10bdd6e-aa94-470f-8bbf-ff27a1d81938	2024-10-14	Warnings	Exact identifier application number: M020
Walgreens Dry Touch Broad Spectrum SPF 55	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	WALGREEN COMPANY	c628b15c-5fd2-fa5a-e053-2a95a90a43ac	2024-10-14	Warnings	Exact identifier application number: M020
Walgreens SPF 30 Hydrating Continuous	AVOBENZONE, HOMOSALATE, OCTOCRYLENE,	WALGREEN COMPANY	c8ae7f1a-d198-6609-e053-2a95a90ad462	2024-10-14	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	Sample	Exclude flag	Status
74154-903-00	74154090300	118 mL in 1 BOTTLE (74154-903-00)	118 ml	2026-02-04	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Kiss My Face Purely Mineral Daily 50 Sunscreen SPF 50	Windmill Health Products, LLC \| Pure Source, LLC	2026-02-25	HUMAN OTC DRUG LABEL	1