Label: OXYMETAZOLINE HYDROCHLORIDE spray, metered
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Contains inactivated NDC Code(s)
NDC Code(s): 64762-864-15, 64762-864-22 - Packager: Dynamic Pharmaceuticals
- 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 December 30, 2009
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Uses
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Warnings
For nasal use only.
Ask a doctor before use if you have
- heart disease
- high blood pressure
- thyroid disease
- diabetes
- trouble urinating due to an enlarged prostate gland
When using this product
- do not use more than directed
- do not use for more than 3 days. Use only as directed.
Frequent or prolonged use may cause nasal congestion to recur or worsen - temporary discomfort such as burning, stinging, sneezing or an increase in nasal discharge may result
- use of this container by more than one person may spread infection
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Directions
- adults and children 6-12 years of age (with adult supervision): Pump 2 or 3 times in each nostril without tilting your head. Sniff deeply. Wipe nozzle clean after use.
- Do not use more often than once every 10 to 12 hours.
- Do not exceed 2 doses in any 24 hour period.
- Children under 6 years of age: consult a doctor
To use pump:
- Remove cap and safety clip.
- Hold with thumb at bottom of bottle and nozzle between fingers.
- Before using the first time, prime pump by depressing several times.
- Other Information
- Inactive Ingredients
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 15 mL Carton
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INGREDIENTS AND APPEARANCE
OXYMETAZOLINE HYDROCHLORIDE
oxymetazoline hydrochloride spray, meteredProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64762-864 Route of Administration NASAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Oxymetazoline Hydrochloride (UNII: K89MJ0S5VY) (Oxymetazoline - UNII:8VLN5B44ZY) Oxymetazoline Hydrochloride 0.2 mg in 0.4 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64762-864-15 1 in 1 CARTON 1 15 mL in 1 BOTTLE, PUMP 2 NDC:64762-864-22 1 in 1 CARTON 2 22 mL in 1 BOTTLE, PUMP Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 11/04/2009 Labeler - Dynamic Pharmaceuticals (617660712) Establishment Name Address ID/FEI Business Operations Dynamic Pharmaceuticals 617660712 MANUFACTURE