Walgreens Maximum Strength Sensitive Fluoride
- Product NDC
- 0363-0631
- 11-digit product format
- 003630631
- Labeler code
- 0363
- Product ID
- 0363-0631_15482811-438f-44dd-97a3-a3d4eb07a609
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Potassium Nitrate and Sodium Fluoride
- Dosage form
- PASTE
- Route
- DENTAL
- Labeler
- Walgreens
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2006-06-06
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM NITRATE; SODIUM FLUORIDE
- Active strength
- 5 mg/g; mg/g
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 0363-0631-09 | Walgreens Maximum Strength Sensitive Fluoride | 113 g in 1 TUBE | PASTE | 113 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-0631 | WALGREENS MAXIMUM STRENGTH SENSITIVE FLUORIDE (POTASSIUM NITRATE AND SODIUM FLUORIDE) PASTE [WALGREENS] | 1 | Legacy NDC, 1 package rows | 20110418_a9585342-fb58-431a-9e16-7b3ca235f6b3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 0363-0631-09 | 00363063109 | 113 g in 1 TUBE | 113 g | Historical |