Label: NO DRIP- oxymetazoline hydrochloride spray
- NDC Code(s): 13709-315-01
- Packager: NeilMed Pharmaceuticals Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 11, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts : Active Ingredients
- Purpose
- Uses
- Warnings
-
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
occur
■ Use of this container by more than one person
may spread infection - STOP USE
- PREGNANCY
- KEEP OUT OF REACH OF CHILDREN
-
Directions
■ Adults and children 6 to under 12 years of age (with adult supervision): 2 or 3 sprays in each nostril not more often than every 10 to 12 hours. Do not exceed 2 doses in any 24-hour period.
■ Children under 6 years of age: ask a doctor To Use: Push firmly down on cap and turn counter clockwise. To spray, squeeze bottle quickly and firmly. Do not tilt head backward while spraying. Wipe nozzle clean after use. Secure cap after use. - Other Information
- Inactive ingredients
-
How to use:
Hold white tabs, SQUEEZE grooved areaofcap FIRMLY and turn counter clockwise. Secure cap after use.Directions
■ Adults and children 6 to under 12 years of age (with adult supervision): 2 or 3 sprays in each nostril not more often than every 10 to 12 hours. Do not exceed 2 doses in any 24-hour period. - No Drip Nasal Spray
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INGREDIENTS AND APPEARANCE
NO DRIP
oxymetazoline hydrochloride sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:13709-315 Route of Administration NASAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY) OXYMETAZOLINE HYDROCHLORIDE 15 mg in 30 mL Inactive Ingredients Ingredient Name Strength EDETATE DISODIUM (UNII: 7FLD91C86K) SODIUM BICARBONATE (UNII: 8MDF5V39QO) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:13709-315-01 1 in 1 CARTON 10/01/2022 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 Drug M012 10/01/2022 Labeler - NeilMed Pharmaceuticals Inc (799295915) Establishment Name Address ID/FEI Business Operations NeilMed Pharmaceuticals Inc 799295915 manufacture(13709-315)