Powder

Product NDC: 61354-117
11-digit product format: 613540117
Labeler code: 61354
Product ID: 61354-117_3e1409fc-06d1-b3a9-e063-6294a90a06e3
Type: HUMAN OTC DRUG
Nonproprietary name: Titanium Dioxide
Dosage form: POWDER
Route: TOPICAL
Labeler: Oxygen Development LLC
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2023-10-27
Substance: FERRIC OXIDE RED; TITANIUM DIOXIDE
Active strength: 1.75; 10 mg/100mg; mg/100mg
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: Powder
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
FERRIC OXIDE RED	1.75 mg/100mg
TITANIUM DIOXIDE	10 mg/100mg

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1K09F3G675	Internal UNII lookup
15FIX9V2JP	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
08b52f29-c1a0-c673-e063-6294a90a9a7a	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
a62a50ac-1535-4461-9768-8ae703e2e9fb	Product name	1	20210525
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877	Product name	1	20140508
bc07ef78-e82d-0c19-31f4-31f263780582	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
61354-117-01	Powder	100 mg in 1 CUP	POWDER	100		3
61354-117-02	Powder	1 in 1 CARTON	POWDER	1		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
61354-117	POWDER (TITANIUM DIOXIDE) POWDER [OXYGEN DEVELOPMENT LLC]	2	Current NDC, 2 package rows	20250508_08b52f29-c1a0-c673-e063-6294a90a9a7a.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 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
1K09F3G675	FERRIC OXIDE RED	1309-37-1	FERRIC OXIDE RED
15FIX9V2JP	TITANIUM DIOXIDE	13463-67-7	TITANIUM DIOXIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
61354-117-01	61354011701	100 mg in 1 CUP	100 mg				Historical
61354-117-02	61354011702	1 CUP in 1 CARTON (61354-117-02) / 100 mg in 1 CUP (61354-117-01)	1 cup	2023-10-27	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
PUR 4-in-1 Pressed Mineral Makeup - LINEN MN3	Oxygen Development LLC \| Oxygen Development DR Limited	2025-09-05	HUMAN OTC DRUG LABEL	3