Sinus Severe Ultra Fine Mist
- Product NDC
- 82706-026
- 11-digit product format
- 827060026
- Labeler code
- 82706
- Product ID
- 82706-026_48bf7422-38f0-d4b4-e063-6294a90aa3ab
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Oxymetazoline hydrochloride.
- Dosage form
- AEROSOL, SPRAY
- Route
- NASAL
- Labeler
- VIVUNT PHARMA LLC
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-01-19
- Substance
- OXYMETAZOLINE HYDROCHLORIDE
- Active strength
- .5 mg/mL
- Pharmacologic classes
- Imidazolines [CS], Increased Sympathetic Activity [PE], Vasoconstriction [PE], Vasoconstrictor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sinus Severe Ultra Fine Mist
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OXYMETAZOLINE HYDROCHLORIDE | .5 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | K89MJ0S5VY |
| Rxcui | 1000990 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82706-026-01 | Sinus Severe Ultra Fine Mist | 15 mL in 1 BOTTLE, SPRAY | AEROSOL, SPRAY | 15 | | 1 |
| 82706-026-01 | Sinus Severe Ultra Fine Mist | 1 in 1 CARTON | AEROSOL, SPRAY | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 82706-026-01 | 82706002601 | 1 BOTTLE, SPRAY in 1 CARTON (82706-026-01) / 15 mL in 1 BOTTLE, SPRAY | 2026-01-19 | No | No | Current |