Label: SEVERE ANEFRIN- oxymetazoline hydrochloride liquid
- NDC Code(s): 0363-2021-15
- Packager: WALGREENS
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- Warnings Ask a doctor before use if you have
-
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 nasla congestion to recur or worsen. • temporary discomfort such as burning, stinging, sneezing or an increase in nasla discharge may occur • use of this container by more than one person may spread infection. Stop use and ask a doctor if symptoms persist
- If Pregnant or breast-feeding,
- Keep out of reach of children.
- Directions
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To Use:
Shake well before use. Hold white tabs, press grooved area of cap firmly and turn counterclockwise. Before using the firsst time, prime metered pump by depressing pump firmly several times. To spray, hold bottle with thumn at base and nozzle between first and second fingers. Without tilting head, insert nozzle into nostril. Fully depress rim with a firm, even stroke and sniff deeply. Wipe nozzle clean after use. Secure cap after use.
- Questions or comments? 1-800-925-4733.
- DISTRIBUTED BY: WALGREENS CO. 200 WILMOT RD., DEERFIELD, IL 60015
- Inactive Ingredients
- Uses
- PURPOSE
- Severe Anefrin Nasal Spray
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INGREDIENTS AND APPEARANCE
SEVERE ANEFRIN
oxymetazoline hydrochloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-2021 Route of Administration NASAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY) OXYMETAZOLINE HYDROCHLORIDE 0.05 g in 15 mL Inactive Ingredients Ingredient Name Strength EDETATE DISODIUM (UNII: 7FLD91C86K) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) EUCALYPTOL (UNII: RV6J6604TK) GLYCERIN (UNII: PDC6A3C0OX) MENTHOL, (+)- (UNII: C6B1OE8P3W) PEG-6 STEARATE (UNII: 8LQC57C6B0) CAMPHOR, (-)- (UNII: 213N3S8275) POVIDONE K30 (UNII: U725QWY32X) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM PHOSPHATE, DIBASIC, MONOHYDRATE (UNII: BWZ7K44R51) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-2021-15 1 in 1 BOTTLE, SPRAY 02/08/2021 12/31/2023 1 15 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 02/08/2021 Labeler - WALGREENS (008965063)