HEB Sensitive Extra Whitening Twin
- Product NDC
- 37808-237
- 11-digit product format
- 378080237
- Labeler code
- 37808
- Product ID
- 37808-237_45775048-8a86-3867-e063-6294a90a6dd2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- ORAL
- Labeler
- HEB
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-12-01
- Substance
- POTASSIUM NITRATE; SODIUM FLUORIDE
- Active strength
- 5; .15 g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- HEB Sensitive Extra Whitening Twin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POTASSIUM NITRATE | 5 g/100g |
| SODIUM FLUORIDE | .15 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | RU45X2JN0Z, 8ZYQ1474W7 |
| Rxcui | 1038929 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 37808-237-10 | HEB Sensitive Extra Whitening Twin | 96.4 g in 1 TUBE | PASTE, DENTIFRICE | 96.4 | | 2 |
| 37808-237-10 | HEB Sensitive Extra Whitening Twin | 2 in 1 CARTON | PASTE, DENTIFRICE | 2 | | 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 |
|---|
| 37808-237-10 | 37808023710 | 2 TUBE in 1 CARTON (37808-237-10) / 96.4 g in 1 TUBE | 2 tube | 2025-12-01 | No | No | Historical |