YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW
- Product NDC
- 59735-182
- 11-digit product format
- 597350182
- Labeler code
- 59735
- Product ID
- 59735-182_4fafb5d1-b38a-dc2e-e063-6394a90a2ce0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- YOUR NAME MINERAL SHEER TINT
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- PML NYC, LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2011-02-01
- Substance
- ZINC OXIDE; TITANIUM DIOXIDE
- Active strength
- 5; 5 g/30mL; g/30mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 59735-182 | I | Inactivated by FDA | 2026-10-21 | ||
| excluded package | package | 59735-182 | 59735-182-01 | I | Inactivated by FDA | 2026-10-21 | |
| excluded package | package | 59735-182 | 59735-182-04 | I | Inactivated by FDA | 2026-10-21 | |
| excluded package | package | 59735-182 | 59735-182-06 | I | Inactivated by FDA | 2026-10-21 | |
| excluded package | package | 59735-182 | 59735-182-08 | I | Inactivated by FDA | 2026-10-21 |
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
- YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ZINC OXIDE | 5 g/30mL |
| TITANIUM DIOXIDE | 5 g/30mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| SOI2LOH54Z | Internal UNII lookup |
| 15FIX9V2JP | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 316c5d69-46f4-7677-e063-6294a90a610f | Available on FDA.report |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59735-182-09 | YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW | 30 mL in 1 TUBE | CREAM | 30 | 8 | |
| 59735-182-10 | YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW | 1 in 1 CARTON | CREAM | 1 | 8 | |
| 59735-182-01 | YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW | 30 mL in 1 TUBE | CREAM | 30 | 6 | |
| 59735-182-01 | YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW | 1 in 1 CARTON | CREAM | 1 | 6 | |
| 59735-182-03 | YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW | 30 mL in 1 TUBE | CREAM | 30 | 6 | |
| 59735-182-04 | YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW | 1 in 1 CARTON | CREAM | 1 | 6 | |
| 59735-182-05 | YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW | 30 mL in 1 TUBE | CREAM | 30 | 6 | |
| 59735-182-06 | YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW | 1 in 1 CARTON | CREAM | 1 | 6 | |
| 59735-182-07 | YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW | 30 mL in 1 TUBE | CREAM | 30 | 6 | |
| 59735-182-08 | YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW | 1 in 1 CARTON | CREAM | 1 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 59735-182 | YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW (YOUR NAME MINERAL SHEER TINT) CREAM [MANA PRODUCT, INC] | 7 | Current NDC, 2 package rows | 20250331_316c5d69-46f4-7677-e063-6294a90a610f.zip |
| 59735-182 | YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW (YOUR NAME MINERAL SHEER TINT) CREAM [MANA PRODUCT, INC] | 6 | Current NDC, 8 package rows | 20240808_0e24934c-b25e-51ef-e063-6394a90a2e3f.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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| SHADED | TITANIUM DIOXIDE, ZINC OXIDE | Potency No. 710 LLC | 31177bbd-68b0-8b24-e063-6294a90aa8d8 | 2025-12-10 | Warnings | M020 |
| SHADED | TITANIUM DIOXIDE, ZINC OXIDE | Potency No. 710 LLC | 3117e138-83a1-0931-e063-6394a90abe43 | 2025-12-10 | Warnings | M020 |
| SHADED | TITANIUM DIOXIDE, ZINC OXIDE | Potency No. 710 LLC | 31188175-a4ca-449f-e063-6394a90a3c05 | 2025-12-10 | Warnings | M020 |
| COVERED | ZINC OXIDE | Potency No. 710 LLC | 3118c3ed-f0f0-f997-e063-6294a90a53a9 | 2025-12-10 | Warnings | M020 |
| COVERED | ZINC OXIDE | Potency No. 710 LLC | 3117faeb-1792-1b2e-e063-6294a90a92df | 2025-12-10 | Warnings | M020 |
| Non-Tinted Mineral Foaming Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | Restore Skin Therapy, LLC | 364b6af2-a0ed-4a17-e063-6394a90a3a17 | 2025-12-10 | M020 | |
| Morning Replenish | ZINC OXIDE | Restore Skin Therapy, LLC | 364b26c2-a1bb-9660-e063-6294a90a14d1 | 2025-12-10 | M020 | |
| Glass Skin Sunscreen Tinted | ZINC OXIDE | Fleur de Lune, LLC | 34288989-35b8-3aa3-e063-6394a90ac2c4 | 2025-12-10 | M020 | |
| Glass Skin Sunscreen Tinted | ZINC OXIDE | Fleur de Lune, LLC | 3418394b-fede-65ce-e063-6394a90ad5f9 | 2025-12-10 | M020 | |
| Glass Skin Sunscreen Non-Tinted | ZINC OXIDE | Fleur de Lune, LLC | 341871e5-c170-7560-e063-6394a90a8eee | 2025-12-10 | M020 | |
| Glass Skin Sunscreen Non-Tinted | ZINC OXIDE | Fleur de Lune, LLC | 3428bdbb-1f18-a29b-e063-6294a90addbc | 2025-12-10 | M020 | |
| Sheer Facial Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | BB MEDICAL & DERMATOLOGY INC | 342b2403-4f4a-3e77-e063-6294a90a4f0a | 2025-12-10 | M020 | |
| Sheer Mineral Sunscreen Bar | TITANIUM DIOXIDE, ZINC OXIDE | BB MEDICAL & DERMATOLOGY INC | 342b69d5-f0e1-99cd-e063-6294a90abb6e | 2025-12-10 | M020 | |
| Sheer Facial Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | BB MEDICAL & DERMATOLOGY INC | 342c3f42-c17f-f777-e063-6394a90a8058 | 2025-12-10 | M020 | |
| Lip SPF | TITANIUM DIOXIDE, ZINC OXIDE | FRANCISCO FLORES, M.D., P.A. | 396d3fdd-99d8-77e8-e063-6294a90aec2f | 2025-12-10 | M020 | |
| Non-Tinted Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | FRANCISCO FLORES, M.D., P.A. | 396cae82-7641-e1b2-e063-6394a90a7c07 | 2025-12-10 | M020 | |
| Solar Knight SPF 40 Broad Spectrum | TITANIUM DIOXIDE, ZINC OXIDE | MASCARENAS ENTERPRISES, INC. | 36c27c91-22ac-205c-e063-6294a90ab379 | 2025-12-10 | M020 | |
| Tinted Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | FRANCISCO FLORES, M.D., P.A. | 396ce15a-06ad-4055-e063-6294a90a27fb | 2025-12-10 | M020 | |
| Dermablue Daily Replenishing | ZINC OXIDE | Dermablue, P.C. | 308da9c9-544e-d5d1-e063-6294a90aa49b | 2025-12-10 | Warnings | M020 |
| Recoverie Mineral Matte | ZINC OXIDE | Clear Day Acne Clinic | 308f41de-fb14-40f9-e063-6394a90a008f | 2025-12-10 | Warnings | M020 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 59735-182-01 | 59735018201 | 30 mL in 1 TUBE | 30 ml | Historical | |||
| 59735-182-03 | 59735018203 | 30 mL in 1 TUBE | 30 ml | Historical | |||
| 59735-182-04 | 59735018204 | 1 in 1 CARTON | Historical | ||||
| 59735-182-05 | 59735018205 | 30 mL in 1 TUBE | 30 ml | Historical | |||
| 59735-182-06 | 59735018206 | 1 in 1 CARTON | Historical | ||||
| 59735-182-07 | 59735018207 | 30 mL in 1 TUBE | 30 ml | Historical | |||
| 59735-182-08 | 59735018208 | 1 in 1 CARTON | Historical | ||||
| 59735-182-09 | 59735018209 | 30 mL in 1 TUBE | 30 ml | Historical | |||
| 59735-182-10 | 59735018210 | 1 TUBE in 1 CARTON (59735-182-10) / 30 mL in 1 TUBE (59735-182-09) | 1 tube | 2011-02-01 | No | No | Current |