White Glo Extreme White Whitening
- Product NDC
- 73656-046
- 11-digit product format
- 736560046
- Labeler code
- 73656
- Product ID
- 73656-046_50b563fb-3816-cc38-e063-6394a90abcf5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM MONOFLUOROPHOSPHATE
- Dosage form
- PASTE, DENTIFRICE
- Route
- TOPICAL
- Labeler
- White Glo USA Inc
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-01-01
- Substance
- SODIUM MONOFLUOROPHOSPHATE
- Active strength
- 7.6 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- White Glo Extreme White Whitening
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM MONOFLUOROPHOSPHATE | 7.6 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | C810JCZ56Q |
| Rxcui | 545626 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73656-046-00 | White Glo Extreme White Whitening | 2 in 1 BOX | PASTE, DENTIFRICE | 2 | | 2 |
| 73656-046-00 | White Glo Extreme White Whitening | 150 g in 1 TUBE | PASTE, DENTIFRICE | 150 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 73656-046-00 | 73656004600 | 2 TUBE in 1 BOX (73656-046-00) / 150 g in 1 TUBE | 2 tube | 2026-01-01 | No | No | Current |