WHITE GLO CHARCOAL SENSITIVE
- Product NDC
- 73656-011
- 11-digit product format
- 736560011
- Labeler code
- 73656
- Product ID
- 73656-011_2f18e9a5-5c1e-c3a8-e063-6294a90a6002
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- POTASSIUM NITRATE, SODIUM MONOFLUOROPHOSPHATE
- Dosage form
- KIT
- Labeler
- WHITE GLO USA INC
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-03-16
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- WHITE GLO CHARCOAL SENSITIVE
- Listing expiration
- 2026-12-31
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73656-011-00 | WHITE GLO CHARCOAL SENSITIVE | 1 in 1 KIT | KIT | 1 | | 6 |
| 73656-012-00 | WHITE GLO CHARCOAL SENSITIVE | 1 in 1 TUBE | PASTE, DENTIFRICE | | 50 mg in 1g | 6 |
| 73656-012-00 | WHITE GLO CHARCOAL SENSITIVE | 150 g in 1 BOX | PASTE, DENTIFRICE | 150 g | 50 mg in 1g | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73656-011 | WHITE GLO CHARCOAL SENSITIVE (POTASSIUM NITRATE, SODIUM MONOFLUOROPHOSPHATE) KIT [WHITE GLO USA INC] | 6 | Current NDC, Legacy NDC, 3 package rows | 20250228_a5edb7fd-c637-5447-e053-2995a90a5a6f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73656-011-00 | 73656001100 | 1 KIT in 1 KIT (73656-011-00) * 1 BOX in 1 TUBE (73656-012-00) / 150 g in 1 BOX | 1 kit | 2020-03-16 | 0000-00-00 | No | No | Current |
| 73656-012-00 | 73656001200 | 1 in 1 TUBE | | | | | | Historical |