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AQUAFRESH
AQUAFRESH - 0135-0179-03 - (sodium fluoride)
Drug Information of AQUAFRESH
| Product NDC: | 0135-0179 |
| Proprietary Name: | AQUAFRESH |
| Non Proprietary Name: | sodium fluoride |
| Active Ingredient(s): | 1.1 mg/g & nbsp; sodium fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AQUAFRESH
| Product NDC: | 0135-0179 |
| Labeler Name: | GlaxoSmithKline Consumer Healthcare LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110325 |
Package Information of AQUAFRESH
| Package NDC: | 0135-0179-03 |
| Package Description: | 1 TUBE in 1 CARTON (0135-0179-03) > 170 g in 1 TUBE |
NDC Information of AQUAFRESH
| NDC Code | 0135-0179-03 |
| Proprietary Name | AQUAFRESH |
| Package Description | 1 TUBE in 1 CARTON (0135-0179-03) > 170 g in 1 TUBE |
| Product NDC | 0135-0179 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | sodium fluoride |
| Dosage Form Name | PASTE |
| Route Name | DENTAL |
| Start Marketing Date | 20110325 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | GlaxoSmithKline Consumer Healthcare LP |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 1.1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
