NDC | 71952-030-00 |
Set ID | 1239e824-aa60-4b7f-9910-81f96ebe6c70 |
Category | HUMAN OTC DRUG LABEL |
Packager | Bee Right LLC |
Generic Name | |
Product Class | alpha-Adrenergic Agonist, beta-Adrenergic Agonist |
Product Number | |
Application Number | PART341 |
- Drug Facts
- Active Ingredient
-
Uses
- temporarily relieves nasal congestion due to the common cold, hay fever (allergic rhinitis)
- temporarily relieves stuffy nose; temporarily restores freer breathing
- reduces swelling of nasal passages; shrinks swollen membranes
- helps decongest sinus openings and passages; temporarily relieves sinus congestion and pressure
- promotes nasal and/or sinus drainage
-
Warnings
Consult a doctor before use if you have:
• heart disease • high blood pressure • thyroid disease • diabetes • difficulty in urination due to enlargement of the prostate gland
When using this product
- use of this container by more than one person may spread infection
- this product may cause temporary discomfort such as burning, stinging, sneezing, or an increase in nasal discharge
- do not use this product for more than 3 days; use only as directed. Frequent or prolonged use may cause nasal congestion to recur or worsen
- Directions
- Other information
- Inactive ingredients
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
RINOSAN MINT NASAL DECONGESTANT
ephedrine hydrochloride sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71952-030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EPHEDRINE HYDROCHLORIDE (UNII: NLJ6390P1Z) (EPHEDRINE - UNII:GN83C131XS) EPHEDRINE HYDROCHLORIDE 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) CALCIUM CHLORIDE (UNII: M4I0D6VV5M) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) EUCALYPTUS OIL (UNII: 2R04ONI662) MENTHOL (UNII: L7T10EIP3A) POTASSIUM CHLORIDE (UNII: 660YQ98I10) SODIUM CHLORIDE (UNII: 451W47IQ8X) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71952-030-00 1 in 1 BOX 07/01/2018 1 30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 07/01/2018 Labeler - Bee Right LLC (080988303)