Label: WALGREEN- nasal spray
- NDC Code(s): 0363-7151-15
- Packager: WALGREENS CO
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 28, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- 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 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 and ask a doctor if
- If pregnant or breast-feeding,
- 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
- Questions or comments?
-
Principal Display Panel
Compare to Afrin® Original* active ingredient††
NDC# 0363-7151-15
NEW Anefrin
Nasal Spray
OXYMETAZOLINE HCL 0.05%
NASAL DECONGESTANT
ORIGINAL
12- HOUR RELIEF
MAXIMUM STRENGTH
- •
- Fast, Powerful Congestion Relief
0.5 FL OZ (15 mL)
TAMPER-EVIDENT: DO NOT USE IF PRINTED SEAL OVER CAP IS BROKEN OR MISSING.
Walgreens Pharmacist Survey
DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD. DERFIELD, IL 60015
100% SATISFACTION GUARANTEED
walgreens.com 2020 © Walgreen Co.
*This product is not manufactured or distributed by Bayer Healthcare LLC, owner of the registered trademark Afrin® Original.
-
INGREDIENTS AND APPEARANCE
WALGREEN
nasal sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-7151 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 100 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) BENZYL ALCOHOL (UNII: LKG8494WBH) EDETATE DISODIUM (UNII: 7FLD91C86K) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM (UNII: GR686LBA74) SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM (UNII: 3980JIH2SW) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-7151-15 1 in 1 CARTON 01/29/2020 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 01/29/2020 Labeler - WALGREENS CO (008965063)
