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NDC 69842-0628-12 EXTRA STRENGTH HEARTBURN RELIEF 254; 237.5 mg/5mL; mg/5mL Details
EXTRA STRENGTH HEARTBURN RELIEF 254; 237.5 mg/5mL; mg/5mL
EXTRA STRENGTH HEARTBURN RELIEF is a ORAL SUSPENSION in the HUMAN OTC DRUG category. It is labeled and distributed by CVS PHARMACY,INC.. The primary component is ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE.
Product Information
| NDC | 69842-0628 |
|---|---|
| Product ID | 69842-628_09079688-4a35-fb60-e063-6394a90ae488 |
| Associated GPIs | |
| 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 | EXTRA STRENGTH HEARTBURN RELIEF |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | aluminum hydroxide and magnesium carbonate |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | SUSPENSION |
| Route | ORAL |
| Active Ingredient Strength | 254; 237.5 |
| Active Ingredient Units | mg/5mL; mg/5mL |
| Substance Name | ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE |
| Labeler Name | CVS PHARMACY,INC. |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M001 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 69842-0628-12 (69842062812)
| NDC Package Code | 69842-628-12 |
|---|---|
| Billing NDC | 69842062812 |
| Package | 355 mL in 1 BOTTLE (69842-628-12) |
| Marketing Start Date | 2017-02-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |