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NDC 00135-0605-01 AQUAFRESH 50; 1.1 mg/g; mg/g Details
AQUAFRESH 50; 1.1 mg/g; mg/g
AQUAFRESH is a DENTAL PASTE in the HUMAN OTC DRUG category. It is labeled and distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC. The primary component is POTASSIUM NITRATE; SODIUM FLUORIDE.
Product Information
| NDC | 00135-0605 |
|---|---|
| Product ID | 0135-0605_2c831976-6b78-48b0-9c0f-64d8b453f36e |
| Associated GPIs | 97503000004400 |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | AQUAFRESH |
| Proprietary Name Suffix | SENSITIVE MAXIMUM STRENGTH |
| Non-Proprietary Name | potassium nitrate and sodium fluoride |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | PASTE |
| Route | DENTAL |
| Active Ingredient Strength | 50; 1.1 |
| Active Ingredient Units | mg/g; mg/g |
| Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
| Labeler Name | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part356 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00135-0605-01 (00135060501)
| NDC Package Code | 0135-0605-01 |
|---|---|
| Billing NDC | 00135060501 |
| Package | 1 TUBE in 1 CARTON (0135-0605-01) / 158.8 g in 1 TUBE |
| Marketing Start Date | 2017-02-17 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |