NDC 59735-920-01 - Amazonian Clay BB Tinted Moisturizer Broad Spectrum SPF 20 Sunscreen Ivory
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 59735-920
- Requested NDC
- 59735-920-01
- Package NDCs from labels
- 59735-920-01, 59735-920-02
- Manufacturer
- PML NYC, LLC
- Effective date
- 2026-04-15
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Titanium Dioxide and Zinc Oxide - PML NYC, LLC | PML NYC, LLC | 2026-04-15 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59735-920-01 | Amazonian Clay BB Tinted Moisturizer Broad Spectrum SPF 20 SunscreenTan-Deep | 50 mL in 1 TUBE | CREAM | 50 | 8 | |
| 59735-920-02 | Amazonian Clay BB Tinted Moisturizer Broad Spectrum SPF 20 SunscreenTan-Deep | 1 in 1 CARTON | CREAM | 1 | 8 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 59735-920 | AMAZONIAN CLAY BB TINTED MOISTURIZER BROAD SPECTRUM SPF 20 SUNSCREEN IVORY (TITANIUM DIOXIDE AND ZINC OXIDE) CREAM AMAZONIAN CLAY BB TINTED MOISTURIZER BROAD SPECTRUM SPF 20 SUNSCREEN LIGHT (TITANIUM DIOXIDE AND ZINC OXIDE) CREAM AMAZONIAN CLAY BB TINTED MOISTURIZER BROAD SPECTRUM SPF 20 SUNSCREEN LIGHT-MEDIUM (TITANIUM DIOXIDE AND ZINC OXIDE) CREAM AMAZONIAN CLAY BB TINTED MOISTURIZER BROAD SPECTRUM SPF 20 SUNSCREEN MEDIUM (TITANIUM DIOXIDE AND ZINC OXIDE) CREAM AMAZONIAN CLAY BB TINTED MOISTURIZER BROAD SPECTRUM SPF 20 SUNSCREEN MEDIUM-TAN (TITANIUM DIOXIDE AND ZINC OXIDE) CREAM AMAZONIAN CLAY BB TINTED MOISTURIZER BROAD SPECTRUM SPF 20 SUNSCREEN TAN (TITANIUM DIOXIDE AND ZINC OXIDE) CREAM AMAZONIAN CLAY BB TINTED MOISTURIZER BROAD SPECTRUM SPF 20 SUNSCREEN TAN-DEEP (TITANIUM DIOXIDE AND ZINC OXIDE) CREAM [MANA PRODUCTS, INC] | 6 | Current NDC, 2 package rows | 20240906_1be639a8-179a-7015-e063-6394a90ab64b.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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.