SinuCleanse Squeeze
- Product NDC
- 42829-405
- 11-digit product format
- 428290405
- Labeler code
- 42829
- Product ID
- 42829-405_2d0731aa-6658-a015-e063-6294a90a807d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM BICARBONATE, SODIUM CHLORIDE
- Dosage form
- KIT
- Route
- NASAL
- Labeler
- ASCENT CONSUMER PRODUCTS, INC.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2015-02-01
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SinuCleanse Squeeze
- Listing expiration
- 2026-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 1542919 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42829-401-01 | SinuCleanse Squeeze | 3000 mg in 1 PACKET | POWDER, FOR SOLUTION | 90000 mg | 700 mg in 3000mg | 9 |
| 42829-405-30 | SinuCleanse Squeeze | 1 in 1 KIT | KIT | 1 | | 9 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| SODIUM BICARBONATE | ACTIVE INGREDIENT | 8MDF5V39QO | SINUCLEANSE SQUEEZE (SODIUM BICARBONATE, SODIUM CHLORIDE) KIT [ASCENT CONSUMER PRODUCTS, INC.] | 4 | |
| SODIUM CHLORIDE | ACTIVE INGREDIENT | 451W47IQ8X | SINUCLEANSE SQUEEZE (SODIUM BICARBONATE, SODIUM CHLORIDE) KIT [ASCENT CONSUMER PRODUCTS, INC.] | 4 | |
| BICARBONATE ION | ACTIVE MOIETY | HN1ZRA3Q20 | SINUCLEANSE SQUEEZE (SODIUM BICARBONATE, SODIUM CHLORIDE) KIT [ASCENT CONSUMER PRODUCTS, INC.] | 4 | |
| SODIUM CATION | ACTIVE MOIETY | LYR4M0NH37 | SINUCLEANSE SQUEEZE (SODIUM BICARBONATE, SODIUM CHLORIDE) KIT [ASCENT CONSUMER PRODUCTS, INC.] | 4 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42829-405 | SINUCLEANSE SQUEEZE (SODIUM BICARBONATE, SODIUM CHLORIDE) KIT [ASCENT CONSUMER PRODUCTS, INC.] | 9 | Current NDC, Legacy NDC, 2 package rows | 20250202_e8f7ea0b-0838-40ac-af1c-6a5ca7afbebe.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42829-401-01 | 42829040101 | 3000 mg in 1 PACKET | 3000 mg | | | | | Historical |
| 42829-405-30 | 42829040530 | 1 KIT in 1 KIT (42829-405-30) * 3000 mg in 1 PACKET (42829-401-01) | 1 kit | 2015-02-01 | 0000-00-00 | No | No | Current |