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 | 2026-11-13 | ||
| excluded package | package | 59735-182 | 59735-182-01 | I | Inactivated by FDA | 2026-11-13 | |
| excluded package | package | 59735-182 | 59735-182-04 | I | Inactivated by FDA | 2026-11-13 | |
| excluded package | package | 59735-182 | 59735-182-06 | I | Inactivated by FDA | 2026-11-13 | |
| excluded package | package | 59735-182 | 59735-182-08 | I | Inactivated by FDA | 2026-11-13 |
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 |
|---|---|---|---|---|---|---|
| Leg Body Makeup | OCTISALATE, OCTOCRYLENE | COSMAX USA, CORPORATION | 06ab109e-abcf-0861-e063-6394a90a9375 | 2024-12-25 | Warnings | M020 |
| Leg Body Makeup | OCTISALATE, OCTOCRYLENE | COSMAX USA, CORPORATION | 0d3379ba-465d-a889-e063-6394a90aaf23 | 2024-12-25 | Warnings | M020 |
| Leg Body Makeup | OCTISALATE, OCTOCRYLENE | COSMAX USA, CORPORATION | 0d339273-6d82-0979-e063-6394a90a3de7 | 2024-12-25 | Warnings | M020 |
| Leg Body Makeup | OCTISALATE, OCTOCRYLENE | COSMAX USA, CORPORATION | 0cc97b34-e9e6-ef6a-e063-6394a90aee89 | 2024-12-25 | Warnings | M020 |
| Leg Body Makeup | OCTISALATE, OCTOCRYLENE | COSMAX USA, CORPORATION | 0cc9760b-b88b-f291-e063-6294a90a242f | 2024-12-25 | Warnings | M020 |
| Leg Body Makeup | OCTISALATE, OCTOCRYLENE | COSMAX USA, CORPORATION | 0d338ec2-dca0-e032-e063-6394a90a69aa | 2024-12-25 | Warnings | M020 |
| Leg Body Makeup | OCTISALATE, OCTOCRYLENE | COSMAX USA, CORPORATION | 0752d79d-5d82-0367-e063-6394a90a4f1c | 2024-12-25 | Warnings | M020 |
| Leg Body Makeup | OCTISALATE, OCTOCRYLENE | COSMAX USA, CORPORATION | 0d33888d-20b3-f912-e063-6394a90a25dc | 2024-12-25 | Warnings | M020 |
| Leg Body Makeup | OCTISALATE, OCTOCRYLENE | COSMAX USA, CORPORATION | 0d3379ba-465c-a889-e063-6394a90aaf23 | 2024-12-25 | Warnings | M020 |
| Buildable Blur | HOMOSALATE, OCTISALATE, ZINC OXIDE | COSMAX USA, CORPORATION | 06b25290-33a0-bafd-e063-6394a90a7a94 | 2024-12-25 | Warnings | M020 |
| Leg Body Makeup | OCTISALATE, OCTOCRYLENE | COSMAX USA, CORPORATION | 0751b356-607f-f3cb-e063-6294a90a4092 | 2024-12-25 | Warnings | M020 |
| Buildable Blur | HOMOSALATE, OCTISALATE, ZINC OXIDE | COSMAX USA, CORPORATION | 06b14a17-cace-1b3e-e063-6394a90afe5d | 2024-12-25 | Warnings | M020 |
| Leg Body Makeup | OCTISALATE, OCTOCRYLENE | COSMAX USA, CORPORATION | 07530636-cd21-3022-e063-6394a90a89d6 | 2024-12-25 | Warnings | M020 |
| Leg Body Makeup | OCTISALATE, OCTOCRYLENE | COSMAX USA, CORPORATION | 0752753e-cac9-9166-e063-6394a90a4d8d | 2024-12-25 | Warnings | M020 |
| Buildable Blur | HOMOSALATE, OCTISALATE, ZINC OXIDE | COSMAX USA, CORPORATION | 06ad3c09-9f1b-b25c-e063-6294a90aebe1 | 2024-12-25 | Warnings | M020 |
| Buildable Blur | HOMOSALATE, OCTISALATE, ZINC OXIDE | COSMAX USA, CORPORATION | 06c57ff5-7013-d35f-e063-6394a90a6ee2 | 2024-12-25 | Warnings | M020 |
| Buildable Blur | HOMOSALATE, OCTISALATE, ZINC OXIDE | COSMAX USA, CORPORATION | 06b1f8bc-8b29-451a-e063-6294a90a34bd | 2024-12-25 | Warnings | M020 |
| Buildable Blur | HOMOSALATE, OCTISALATE, ZINC OXIDE | COSMAX USA, CORPORATION | 06b26dd0-44de-91a7-e063-6394a90a603a | 2024-12-25 | Warnings | M020 |
| Buildable Blur | HOMOSALATE, OCTISALATE, ZINC OXIDE | COSMAX USA, CORPORATION | 06b26dd0-44ef-91a7-e063-6394a90a603a | 2024-12-25 | Warnings | M020 |
| Buildable Blur | HOMOSALATE, OCTISALATE, ZINC OXIDE | COSMAX USA, CORPORATION | 06b25290-33a3-bafd-e063-6394a90a7a94 | 2024-12-25 | 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 |