NDC 57353-103-13 - LUSTER NOW INSTANT WHITENING
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
- 57353-103
- Requested NDC
- 57353-103-13
- Package NDCs from labels
- 57353-103-13, 57353-103-53, 57353-103-11, 57353-103-31
- Manufacturer
- DENTOVATIONS INC | Lornamead Inc.
- Effective date
- 2019-02-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Luster Now Instant Whitening Toothpaste | DENTOVATIONS INC | Lornamead Inc. | 2019-02-26 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 57353-103-31 | 2020-09-27 | Luster Now Instant Whitening Toothpaste |
| 57353-103-53 | 2020-09-27 | Luster Now Instant Whitening Toothpaste |
| 57353-103-31 | 2020-09-25 | Luster Now Instant Whitening Toothpaste |
| 57353-103-53 | 2020-09-25 | Luster Now Instant Whitening Toothpaste |
| 57353-103-31 | 2020-07-22 | Luster Now Instant Whitening Toothpaste |
| 57353-103-53 | 2020-07-22 | Luster Now Instant Whitening Toothpaste |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 57353-103-11 | LUSTER NOWINSTANT WHITENING | 42 g in 1 TUBE | GEL, DENTIFRICE | 42 | 5 | |
| 57353-103-13 | LUSTER NOWINSTANT WHITENING | 113 g in 1 TUBE | GEL, DENTIFRICE | 113 | 5 | |
| 57353-103-31 | LUSTER NOWINSTANT WHITENING | 3 in 1 BOX | GEL, DENTIFRICE | 3 | 5 | |
| 57353-103-53 | LUSTER NOWINSTANT WHITENING | 1 in 1 BOX | GEL, DENTIFRICE | 1 | 5 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
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.