WALGREENS
- Product NDC
- 0363-1834
- 11-digit product format
- 003631834
- Labeler code
- 0363
- Product ID
- 0363-1834_2de7ff66-af75-4d9d-b493-29b37dadc5d8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium citrate dihydrate
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- WALGREENS CO.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2025-12-29
- Substance
- TRISODIUM CITRATE DIHYDRATE
- Active strength
- 230 mg/1
- Pharmacologic classes
- Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- WALGREENS
- Brand name suffix
- UPSET STOMACH and NAUSEA RELIEF
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TRISODIUM CITRATE DIHYDRATE | 230 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | B22547B95K |
| Rxcui | 2002800 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0363-1834-42 | WALGREENSUPSET STOMACH and NAUSEA RELIEF | 1 in 1 BOX | TABLET, CHEWABLE | 1 | | 1 |
| 0363-1834-42 | WALGREENSUPSET STOMACH and NAUSEA RELIEF | 42 in 1 BOTTLE | TABLET, CHEWABLE | 42 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0363-1834-42 | 00363183442 | 1 BOTTLE in 1 BOX (0363-1834-42) / 42 TABLET, CHEWABLE in 1 BOTTLE | 1 bottle | 2025-12-29 | No | No | Current |