RESP EASE
- Product NDC
- 43014-1114
- 11-digit product format
- 430141114
- Labeler code
- 43014
- Product ID
- 43014-1114_4d27a1b8-77e8-0707-e063-6294a90a5565
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM CHLORIDE
- Dosage form
- LIQUID
- Route
- NASAL
- Labeler
- Laboratoire Unither
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2025-04-01
- Substance
- SODIUM CHLORIDE
- Active strength
- 70 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- RESP EASE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM CHLORIDE | 70 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 451W47IQ8X |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 43014-1114-1 | RESP EASE | 25 in 1 CARTON | LIQUID | 25 | | 2 |
| 43014-1114-1 | RESP EASE | 5 mL in 1 VIAL | LIQUID | 5 | | 2 |
| 43014-1114-2 | RESP EASE | 4 mL in 1 VIAL | LIQUID | 4 | | 2 |
| 43014-1114-2 | RESP EASE | 60 in 1 CARTON | LIQUID | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43014-1114 | RESP EASE (SODIUM CHLORIDE) LIQUID [LABORATOIRE UNITHER] | 1 | Current NDC, 4 package rows | 20250403_31b8dcbd-9e6b-1edc-e063-6394a90aac73.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 43014-1114-1 | 43014111401 | 25 VIAL in 1 CARTON (43014-1114-1) / 5 mL in 1 VIAL | 25 vial | 2025-04-01 | No | No | Current |
| 43014-1114-2 | 43014111402 | 60 VIAL in 1 CARTON (43014-1114-2) / 4 mL in 1 VIAL | 60 vial | 2026-03-15 | No | No | Current |