ZEROQ
- Product NDC
- 80643-0002
- 11-digit product format
- 806430002
- Labeler code
- 80643
- Product ID
- 80643-0002_b0620ffa-d34c-1917-e053-2995a90a84b4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Potassium carbonate
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- JISANG Co., Ltd.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-09-21
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CARBONATE
- Active strength
- 1 g/500mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 80643-0002-1 | ZEROQ | 500 mL in 1 BOTTLE, SPRAY | LIQUID | 500 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 80643-0002 | ZEROQ (POTASSIUM CARBONATE) LIQUID [JISANG CO., LTD.] | 1 | Legacy NDC, 1 package rows | 20200929_b061d3e7-51c9-048c-e053-2995a90af53f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 80643-0002-1 | 80643000201 | 500 mL in 1 BOTTLE, SPRAY (80643-0002-1) | 500 ml | 2020-09-21 | 0000-00-00 | No | No | Current |