EasyStick
- Product NDC
- 75124-0004
- 11-digit product format
- 751240004
- Labeler code
- 75124
- Product ID
- 75124-0004_0a4eb0be-cd46-6702-e063-6294a90ab9a3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- sodium chlorite
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Pure O2
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-04-01
- Substance
- SODIUM CHLORITE
- Active strength
- 5 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
- EasyStick
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM CHLORITE | 5 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | G538EBV4VF |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 75124-0004-1 | EasyStick | 9 g in 1 PACKAGE | LIQUID | 9 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 75124-0004 | EASYSTICK (SODIUM CHLORITE) LIQUID [PURE O2] | 3 | Current NDC, Legacy NDC, 1 package rows | 20231117_a39b9ce6-a074-4165-e053-2995a90a277a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 75124-0004-1 | 75124000401 | 9 g in 1 PACKAGE (75124-0004-1) | 9 g | 2020-04-01 | 0000-00-00 | No | No | Current |