Label: RINOSAN PROPO NASAL DECONGESTANT- ephedrine hydrochloride spray
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Contains inactivated NDC Code(s)
NDC Code(s): 71952-040-00 - Packager: Bee Right LLC
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated July 3, 2018
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
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Uses
- temporarily relieves nasal congestion due to the common cold, hay fever (allergic rhinitis)
- temporarily relieves stuffy nose
- temporarily restores freer breathing through the nose
- reduces swelling of nasal passages; shrinks swollen membranes
- helps decongest sinus openings and passages;
- promotes nasal and/or sinus drainage; temporarily relieves sinus congestion and pressure
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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:
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INGREDIENTS AND APPEARANCE
RINOSAN PROPO NASAL DECONGESTANT
ephedrine hydrochloride sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71952-040 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 GLYCERIN (UNII: PDC6A3C0OX) SODIUM CHLORIDE (UNII: 451W47IQ8X) WATER (UNII: 059QF0KO0R) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71952-040-00 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)