PURISTIC
- Product NDC
- 82422-001
- 11-digit product format
- 824220001
- Labeler code
- 82422
- Product ID
- 82422-001_d1bb2aed-302b-6907-e053-2995a90adcde
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium chlorite
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- MEDI K Co., Ltd.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2021-11-27
- Marketing end
- 0000-00-00
- Substance
- SODIUM CHLORITE
- Active strength
- 5 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 82422-001-01 | PURISTIC | 6 mL in 1 BOTTLE | LIQUID | 6 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82422-001 | PURISTIC (SODIUM CHLORITE) LIQUID [MEDI K CO., LTD.] | 1 | Legacy NDC, 1 package rows | 20211128_d1bb2aed-302a-6907-e053-2995a90adcde.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 82422-001-01 | 82422000101 | 6 mL in 1 BOTTLE (82422-001-01) | 6 ml | 2021-11-27 | 0000-00-00 | No | No | Current |