Search by Drug Name or NDC
NDC 00135-0094-42 GAVISCON 95; 358 mg/15mL; mg/15mL Details
GAVISCON 95; 358 mg/15mL; mg/15mL
GAVISCON is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC. The primary component is ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE.
Product Information
| NDC | 00135-0094 |
|---|---|
| Product ID | 0135-0094_0ab338be-56a6-284d-e063-6294a90a306f |
| Associated GPIs | 48990002151809 |
| GCN Sequence Number | 048731 |
| GCN Sequence Number Description | mag carb/aluminum hydrox/algin ORAL SUSP 358-95/15 ORAL |
| HIC3 | D4B |
| HIC3 Description | ANTACIDS |
| GCN | 14196 |
| HICL Sequence Number | 001172 |
| HICL Sequence Number Description | MAGNESIUM CARBONATE/ALUMINUM HYDROXIDE/ALGINIC ACID |
| Brand/Generic | Brand |
| Proprietary Name | GAVISCON |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | aluminum hydroxide and magnesium carbonate |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | LIQUID |
| Route | ORAL |
| Active Ingredient Strength | 95; 358 |
| Active Ingredient Units | mg/15mL; mg/15mL |
| Substance Name | ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE |
| Labeler Name | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M001 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00135-0094-42 (00135009442)
| NDC Package Code | 0135-0094-42 |
|---|---|
| Billing NDC | 00135009442 |
| Package | 177 mL in 1 BOTTLE (0135-0094-42) |
| Marketing Start Date | 2011-01-14 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |