Soothe
- Product NDC
- 0363-7370
- 11-digit product format
- 003637370
- Labeler code
- 0363
- Product ID
- 0363-7370_931dd60d-ef3f-4395-8bf3-3dd11676a6d0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bismuth subsalicylate
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Walgreens
- Application
- M008
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-01-31
- Substance
- BISMUTH SUBSALICYLATE
- Active strength
- 525 mg/15mL
- Pharmacologic classes
- Bismuth [CS], Bismuth [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Soothe
- Brand name suffix
- Ultra Strength
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BISMUTH SUBSALICYLATE | 525 mg/15mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 62TEY51RR1 |
| Rxcui | 308763 |
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 |
|---|
| 0363-7370-04 | SootheUltra Strength | 118 mL in 1 BOTTLE, PLASTIC | LIQUID | 118 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-7370 | SOOTHE ULTRA STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [WALGREENS] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240522_ec96e6f2-b087-457e-9b95-30f3595deebb.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 |
|---|
| 0363-7370-04 | 00363737004 | 118 mL in 1 BOTTLE, PLASTIC (0363-7370-04) | 118 ml | 2020-01-31 | 0000-00-00 | No | No | Current |