Sodium Chloride
- Product NDC
- 58657-119
- 11-digit product format
- 586570119
- Labeler code
- 58657
- Product ID
- 58657-119_50266e4c-32ea-0583-e063-6294a90a6ff4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Method Pharmaceuticals, LLC
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-02-13
- Substance
- SODIUM CHLORIDE
- Active strength
- 1 g/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sodium Chloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM CHLORIDE | 1 g/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 451W47IQ8X |
| Rxcui | 313009 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 58657-119-01 | Sodium Chloride | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 58657-119-01 | 58657011901 | 100 TABLET in 1 BOTTLE (58657-119-01) | 100 tablet | 2026-02-13 | No | No | Historical |