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- NDC Code(s): 83324-238-01
- Packager: CHAIN DRUG MARKETING ASSOCIATION
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 19, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
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- Active ingredient
Oxymetazoline hydrochloride 0.05%
- Purpose
Nasal Decongestant
- Uses
- temporarily relief of nasal congestion due to:
- common cold,
- hay fever
- upper respiratory allergies
- temporarily relieves sinus congestion and pressure
- shrinks swollen nasal membranes so you can breathe more freely
- temporarily relief of nasal congestion due to:
- Warnings
- Ask a doctor before use if you have
- heart disease
- high blood pressure
- diabetes
- thyroid disease
- 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 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,
ask a health professional before use.
- Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.
- 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 counterclockwise
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
- store at room temperature
- Keep this carton for future reference on full labeling.
- Inactive ingredients
benzalkonium chloride, benzyl alcohol, edetate disodium, polyethylene glycol, povidone, propylene glycol, purified water, sodium phosphate dibasic, sodium phosphate monobasic.
- Questions or comments?
1-866-467-2748
- Principal Display Panel
QUALITY CHOICE
NDC# 83324-238-01
*Compare to the Active Ingredient in AFRIN® Original Nasal Spray
Nasal Spray
Nasal Decongestant
Oxymetazoline HCl 0.05%
Nasal Solution
Fast, Powerful Congestion Relief
For Colds & Allergies
12 Hour Relief
Original
1 FL OZ (30 mL)
100% QC SATISFACTION GURANTEED
Distributed by C.D.M.A., Inc.©
Novi, MI 48375
Questions: 800-935-2362
*This product is not manufactured or distributed by Bayer Healthcare LLC, distributer of Afrin ®Original.
- INGREDIENTS AND APPEARANCE
QUALITY CHOICENASAL
oxymetazoline hydrochloride sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83324-238 Route of Administration NASAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY) OXYMETAZOLINE HYDROCHLORIDE 0.05g in100mL 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:83324-238-01 1 in 1 CARTON 05/01/2025 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 05/01/2025 Labeler -CHAIN DRUG MARKETING ASSOCIATION(011920774)
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Safety
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Related Resources
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More Info on this Drug
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View Labeling Archives for this drug
QUALITY CHOICE NASAL- oxymetazoline hydrochloride spray
Number of versions: 1
| Published Date (What is this?) | Version | Files |
|---|---|---|
| May 21, 2025 | 1 (current) | download |
RxNorm
QUALITY CHOICE NASAL- oxymetazoline hydrochloride spray
| RxCUI | RxNorm NAME | RxTTY | |
|---|---|---|---|
| 1 | 1000990 | oxymetazoline HCl 0.05 % Nasal Spray | PSN |
| 2 | 1000990 | oxymetazoline hydrochloride 0.5 MG/ML Nasal Spray | SCD |
| 3 | 1000990 | oxymetazoline hydrochloride 0.05 % Nasal Spray | SY |
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QUALITY CHOICE NASAL- oxymetazoline hydrochloride spray
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NDC Codes
QUALITY CHOICE NASAL- oxymetazoline hydrochloride spray
If this SPL contains inactivated NDCs listed by the FDA initiated compliance action, they will be specified as such.
| NDC | |
|---|---|
| 1 | 83324-238-01 |
