Aquafresh
- Product NDC
- 0135-0619
- 11-digit product format
- 001350619
- Labeler code
- 0135
- Product ID
- 0135-0619_bfd08a48-c926-4126-90fb-4a3527ebb678
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- sodium monofluorophosphate
- Dosage form
- PASTE
- Route
- DENTAL
- Labeler
- GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-09-01
- Marketing end
- 0000-00-00
- Substance
- SODIUM MONOFLUOROPHOSPHATE
- Active strength
- 1 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0135-0619-01 | 00135061901 | 130.4 g in 1 CANISTER (0135-0619-01) | 130.4 g | 2017-09-01 | 0000-00-00 | No | No | Current |