Giant Eagle Wintermint Zero Alcohol
- Product NDC
- 63148-022
- 11-digit product format
- 631480022
- Labeler code
- 63148
- Product ID
- 63148-022_3ea64bdf-8ff5-4e62-a4cc-2fdbd0a65b85
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- Apollo Health and Beauty Care Inc.
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-10-21
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 0 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 63148-022-33 | Giant Eagle Wintermint Zero Alcohol | 1000 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 1000 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63148-022 | GIANT EAGLE WINTERMINT ZERO ALCOHOL (SODIUM FLUORIDE) MOUTHWASH [APOLLO HEALTH AND BEAUTY CARE INC.] | 1 | Legacy NDC, 1 package rows | 20191023_a271e0ff-614b-4b8b-9eec-de82c8c12e4d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 63148-022-33 | 63148002233 | 1000 mL in 1 BOTTLE, PLASTIC | 1000 ml | Historical |