DR.ALTHEA WATER GLOW AQUA
- Product NDC
- 70905-0001
- 11-digit product format
- 709050001
- Labeler code
- 70905
- Product ID
- 70905-0001_39d7a5d2-678d-4c08-e054-00144ff8d46c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- PROPOLIS WAX
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Dr. Althea
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2016-08-11
- Marketing end
- 0000-00-00
- Substance
- PROPOLIS WAX
- Active strength
- 0 g/100mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70905-0001-1 | DR.ALTHEA WATER GLOW AQUA | 50 mL in 1 JAR | CREAM | 50 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70905-0001 | DR.ALTHEA WATER GLOW AQUA (PROPOLIS WAX) CREAM [DR. ALTHEA] | 2 | Legacy NDC, 1 package rows | 20160812_b7a7b4dd-dc92-4024-8015-355ed8c00ebd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 70905-0001-1 | 70905000101 | 50 mL in 1 JAR | 50 ml | Historical |