AQUAFRESH
- Product NDC
- 0135-0594
- 11-digit product format
- 001350594
- Labeler code
- 0135
- Product ID
- 0135-0594_40a68f16-fab7-4f4a-a24d-623228dff662
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- sodium fluoride
- Dosage form
- PASTE
- Route
- DENTAL
- Labeler
- GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-01-31
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 1 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0135-0594-01 | AQUAFRESHMULTI ACTION WHITENING | 1 in 1 CARTON | PASTE | 1 | | 9 |
| 0135-0594-01 | AQUAFRESHMULTI ACTION WHITENING | 158.8 g in 1 TUBE | PASTE | 158.8 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0135-0594 | AQUAFRESH CAVITY PROTECTION (SODIUM FLUORIDE) PASTE AQUAFRESH EXTRA FRESH PLUS WHITENING (SODIUM FLUORIDE) PASTE AQUAFRESH MULTI ACTION WHITENING (SODIUM FLUORIDE) PASTE AQUAFRESH ULTIMATE WHITE (SODIUM FLUORIDE) PASTE [HALEON US HOLDINGS LLC] | 8 | Legacy NDC, 2 package rows | 20240301_5484999c-8e6f-430d-99a5-6893a2489467.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0135-0594-01 | 00135059401 | 1 TUBE in 1 CARTON (0135-0594-01) > 158.8 g in 1 TUBE | 1 tube | 2017-01-31 | 0000-00-00 | No | No | Current |