Foot Clean Gold
- Product NDC
- 71059-010
- 11-digit product format
- 710590010
- Labeler code
- 71059
- Product ID
- 71059-010_6f8f71c2-802b-4090-a5e2-afe2cf1efaeb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- PROPOLIS WAX
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- KONEL
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2016-11-01
- Marketing end
- 0000-00-00
- Substance
- PROPOLIS WAX
- Active strength
- 4 g/30g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 71059-010-01 | Foot Clean Gold | 30 g in 1 BOTTLE, PLASTIC | POWDER | 30 | | 3 |
| 71059-010-02 | Foot Clean Gold | 1 in 1 CARTON | POWDER | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71059-010 | FOOT CLEAN GOLD (PROPOLIS WAX) POWDER [KONEL] | 3 | Legacy NDC, 2 package rows | 20221029_0af4ef34-dfa1-4450-8f54-1c0641ebb0ba.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71059-010-01 | 71059001001 | 30 g in 1 BOTTLE, PLASTIC | 30 g | | | | | Historical |
| 71059-010-02 | 71059001002 | 1 BOTTLE, PLASTIC in 1 CARTON (71059-010-02) > 30 g in 1 BOTTLE, PLASTIC (71059-010-01) | | 2016-11-01 | 0000-00-00 | No | No | Current |