Powder

Product NDC
61354-190
11-digit product format
613540190
Labeler code
61354
Product ID
61354-190_4d3a0eae-1e8c-3460-e063-6394a90a8c81
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
2025-07-18
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
IngredientStrength
FERRIC OXIDE RED1.75 mg/100mg
TITANIUM DIOXIDE10 mg/100mg

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1K09F3G675Internal UNII lookup
15FIX9V2JPInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
4d3a0a92-b0de-a1ea-e063-6294a90a8508Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
a62a50ac-1535-4461-9768-8ae703e2e9fbProduct name120210525
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508
bc07ef78-e82d-0c19-31f4-31f263780582Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61354-190-01Powder1 in 1 CARTONPOWDER11
61354-190-01Powder100 mg in 1 CUPPOWDER1001

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 281 of 346 · 6,912 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
H.E.B. Mineral Sunscreen Broad Spectrum SPF 50TITANIUM DIOXIDE, ZINC OXIDEH.E.B.c5279caf-3af9-d163-e053-2995a90a943b2024-10-15WarningsExact identifier
application number: M020
HEB Face 50 Clear Zinc SunscreenOCTOCRYLENE, ZINC OXIDEH.E.B.f6e3c883-0087-dcd6-e053-6394a90a12722024-10-15WarningsExact identifier
application number: M020
HEB Mineral Sunscreen SPF 50ZINC OXIDEH.E.B.de99343b-c74c-3f43-e053-2995a90ac9dd2024-10-15WarningsExact identifier
application number: M020
HEB SPF 55 Babies and Kids SunscreenAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEH.E.B.f5660a97-57c8-61c7-e053-2995a90a01642024-10-15WarningsExact identifier
application number: M020
H.E.BSPF 50 SUNSCREENH.E.B362f726b-d52b-4dae-ade6-a47de47697ef2024-10-15WarningsExact identifier
application number: M020
HEB Sensitive 50 Mineral Sensitive Skin Sunscreen For FaceZINC OXIDEH.E.B.dfb43fc5-4968-f999-e053-2a95a90a08192024-10-15WarningsExact identifier
application number: M020
H.E.B BABYSPF 50 SUNSCREENH.E.B61273611-ab7a-4216-aebe-2c8d896602812024-10-15WarningsExact identifier
application number: M020
H.E.B BANANASPF 50 SUNSCREENH.E.Bb9a9837a-094b-4a57-a50c-5c1437deda7b2024-10-15WarningsExact identifier
application number: M020
HEB Solutions SunscreenSPORT SPF 100 LOTIONH.E.B9e3ea66c-d6a0-49ca-a3c0-8175e06174532024-10-15WarningsExact identifier
application number: M020
H.E.B Solutions SunscreenULTRA SPF 50 LOTIONH.E.B12c76c72-4411-48d5-b79b-c58703bf1fdd2024-10-15WarningsExact identifier
application number: M020
H.E.B Solutions SunscreenSPORT SPF 50 CONTINUOUS SPRAYH.E.B86ad5d30-f700-42a2-b810-dd2e3ed0f2d82024-10-15WarningsExact identifier
application number: M020
H.E.BSPF 50 SUNSCREENH.E.B1f8d4f91-9eb9-41de-9066-a7a08c7ff84f2024-10-15WarningsExact identifier
application number: M020
H.E.B Solutions SunscreenULTRA SPF 100 CONTINUOUS SPRAYH.E.Bbe80244d-da6d-4d37-b228-4d3fac335caf2024-10-15WarningsExact identifier
application number: M020
H.E.B Solutions SunscreenKIDS SPF 50 LOTION SPRAYH.E.B9b43c5d5-c279-4ae3-843e-1451f73242162024-10-15WarningsExact identifier
application number: M020
H.E.B Solutions SunscreenULTRA SPF 50 CONTINUOUS SPRAYH.E.B2e183ba8-1b83-4211-bc08-dbdcee942ce92024-10-15WarningsExact identifier
application number: M020
EQUALINE KIDS SPF 50AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEUnited Natural Foods, Inc. dba UNFIe46cb6e3-ea8d-3c2d-e053-2a95a90a0bf62024-10-15WarningsExact identifier
application number: M020
Mineral SunscreenZINC OXIDE SUNSCREENBentley Laboratories LLC782a8641-7e6a-413b-a2ed-0efeb36c48a72024-10-15WarningsExact identifier
application number: M020
H.E.B MANGOSPF 50 SUNSCREENH.E.B35898f07-2973-461a-91b8-095aa4cf38ee2024-10-15WarningsExact identifier
application number: M020
H.E.B Solutions SunscreenSPORT SPF 30 CONTINUOUS SPRAYH.E.B8b6d0c0d-485b-4428-91e5-5befcac18d5d2024-10-15WarningsExact identifier
application number: M020
H.E.B Solutions SunscreenULTRA SPF 50 CONTINUOUS SPRAYH.E.B5fd3d730-d916-48f4-bb94-62d40d1812802024-10-15WarningsExact identifier
application number: M020

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
61354-190-01613540190011 CUP in 1 CARTON (61354-190-01) / 100 mg in 1 CUP1 cup2025-07-18NoNoCurrent