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NDC 11673-0187-36 Up and Up Antacid and Pain Relief 1000; 325; 1916 mg/1; mg/1; mg/1 Details
Up and Up Antacid and Pain Relief 1000; 325; 1916 mg/1; mg/1; mg/1
Up and Up Antacid and Pain Relief is a ORAL TABLET, EFFERVESCENT in the HUMAN OTC DRUG category. It is labeled and distributed by Target Corporation. The primary component is ANHYDROUS CITRIC ACID; ASPIRIN; SODIUM BICARBONATE.
Product Information
| NDC | 11673-0187 |
|---|---|
| Product ID | 11673-187_f0468186-c3f9-2030-e053-2995a90af3f2 |
| 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 | Up and Up Antacid and Pain Relief |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Aspirin, Citric Acid, Sodium Bicarbonate |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, EFFERVESCENT |
| Route | ORAL |
| Active Ingredient Strength | 1000; 325; 1916 |
| Active Ingredient Units | mg/1; mg/1; mg/1 |
| Substance Name | ANHYDROUS CITRIC ACID; ASPIRIN; SODIUM BICARBONATE |
| Labeler Name | Target Corporation |
| Pharmaceutical Class | Acidifying Activity [MoA], Alkalinizing Activity [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Cyclooxygenase Inhibitors [MoA], Decreased Coagulation Factor Ac |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part343 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 11673-0187-36 (11673018736)
| NDC Package Code | 11673-187-36 |
|---|---|
| Billing NDC | 11673018736 |
| Package | 18 POUCH in 1 CARTON (11673-187-36) / 2 TABLET, EFFERVESCENT in 1 POUCH |
| Marketing Start Date | 2020-06-24 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |