Soothe
- Product NDC
- 0363-0736
- 11-digit product format
- 003630736
- Labeler code
- 0363
- Product ID
- 0363-0736_bbf2fb85-f771-48b4-bc81-efd73b11049a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth subsalicylate
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Walgreens
- Application
- M008
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-11-29
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 525 mg/30mL
- Pharmacologic classes
- Bismuth [CS], Bismuth [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Soothe
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BISMUTH SUBSALICYLATE | 525 mg/30mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 62TEY51RR1 |
| Rxcui | 308762 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0363-0736-16 | Soothe | 473 mL in 1 BOTTLE, PLASTIC | LIQUID | 473 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-0736 | SOOTHE (BISMUTH SUBSALICYLATE) LIQUID [WALGREENS] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240628_450483c3-487f-4a8f-a439-5661241a8f0f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0363-0736-16 | 00363073616 | 473 mL in 1 BOTTLE, PLASTIC (0363-0736-16) | 473 ml | 2019-11-29 | 0000-00-00 | No | No | Current |