ZEROQ FACE BODY
- Product NDC
- 80643-0003
- 11-digit product format
- 806430003
- Labeler code
- 80643
- Product ID
- 80643-0003_b061fcf0-af92-96ff-e053-2a95a90a99fc
- 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
- 0 g/100mL
- 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 |
|---|
| 80643-0003-1 | ZEROQ FACE BODY | 100 mL in 1 BOTTLE, SPRAY | LIQUID | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 80643-0003 | ZEROQ FACE BODY (POTASSIUM CARBONATE) LIQUID [JISANG CO., LTD.] | 1 | Legacy NDC, 1 package rows | 20200929_b062193f-b59a-0b02-e053-2995a90a6b88.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 80643-0003-1 | 80643000301 | 100 mL in 1 BOTTLE, SPRAY (80643-0003-1) | 100 ml | 2020-09-21 | 0000-00-00 | No | No | Current |