QVE - S
- Product NDC
- 75124-0010
- 11-digit product format
- 751240010
- Labeler code
- 75124
- Product ID
- 75124-0010_acde31eb-b011-5f00-e053-2a95a90a36eb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- sodium chlorite
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Pure O2
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-08-15
- Substance
- SODIUM CHLORITE
- Active strength
- 23 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- QVE - S
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM CHLORITE | 23 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | G538EBV4VF |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 75124-0010-1 | QVE - S | 4 g in 1 POUCH | POWDER | 4 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 75124-0010 | QVE - S (SODIUM CHLORITE) POWDER [PURE O2] | 1 | Current NDC, Legacy NDC, 1 package rows | 20200815_acdeca69-4e20-9502-e053-2a95a90a5327.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 75124-0010-1 | 75124001001 | 4 g in 1 POUCH (75124-0010-1) | 4 g | 2020-08-15 | 0000-00-00 | No | No | Current |