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NDC 63868-0565-12 HEARTBURN RELIEF 254; 237.5 mg/5mL; mg/5mL Details
HEARTBURN RELIEF 254; 237.5 mg/5mL; mg/5mL
HEARTBURN RELIEF is a ORAL SUSPENSION in the HUMAN OTC DRUG category. It is labeled and distributed by CHAIN DRUG MARKETING ASSOCIATION. The primary component is ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE.
Product Information
| NDC | 63868-0565 |
|---|---|
| Product ID | 63868-565_097f7264-6848-61fb-e063-6294a90a3f2f |
| 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 | 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 | CHAIN DRUG MARKETING ASSOCIATION |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M001 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 63868-0565-12 (63868056512)
| NDC Package Code | 63868-565-12 |
|---|---|
| Billing NDC | 63868056512 |
| Package | 355 mL in 1 BOTTLE (63868-565-12) |
| Marketing Start Date | 2019-11-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |