PURE SPRING
- Product NDC
- 11822-4650
- 11-digit product format
- 118224650
- Labeler code
- 11822
- Product ID
- 11822-4650_95d28594-88c9-419c-9ab0-395dd8a938bd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ETHYL ALCOHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- RITE AID
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2012-03-01
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 62 mL/100mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 11822-4650-9 | PURE SPRING | 260 mL in 1 BOTTLE, PLASTIC | LIQUID | 260 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-4650 | PURE SPRING (ETHYL ALCOHOL) LIQUID [RITE AID] | 1 | Legacy NDC, 1 package rows | 20120307_23ca18ac-9232-4399-8dc5-6176cddd3e04.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 11822-4650-9 | 11822465009 | 260 mL in 1 BOTTLE, PLASTIC | 260 ml | Historical |