MEDIX NASAL DECONGESTANT OXYMETAZOLINE HYDROCHLORIDE- oxymetazoline hydrochloride liquid 
Medic -33, Inc.

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Medix Nasal Decongestant Oxymetazoline Hydrochloride

Drug Facts

Active ingredient

Oxymetazoline hydrochloride 0.05%

Purpose

nasal decongestant

Uses

Warnings

Do not use

  • this product for more than 3 days. Use only as directed. Frequent or prolonged use may cause nasal congestion to recur or worsen. If symptoms persist, consult a doctor.

Ask a doctor before use if you have

  • heart disease
  • high blood pressure
  • thyroid disease
  • diabetes
  • difficulty in urination due to enlargement of the prostate gland

When using this product

  • do not exceed recommended dosage.
  • this product may cause temporary discomfort such as burning, stinging, sneezing, or an increase in nasal discharge.
  • the use of this container by more than one person may spread infection.

If pregnant or breastfeeding,

ask a health professional before use.

Keep out of reach of children.

If swallowed, get medical help or contact Poison Control Center right away.

Directions

Other information

Do not use if the tamper-proof seal is damaged or broken.

Inactive ingredients

Glutathione, menthol oil, pyrroloquinoline quinine, sodium nitrate, wintergreen oil, water.

Questions or Comments?

305-861-1457

Package Labeling:

Label

MEDIX NASAL DECONGESTANT OXYMETAZOLINE HYDROCHLORIDE 
oxymetazoline hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83522-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY) OXYMETAZOLINE HYDROCHLORIDE0.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLUTATHIONE (UNII: GAN16C9B8O)  
PYRROLOQUINOLINEDIONE TRICARBOXYLIC ACID (UNII: 47819QGH5L)  
SODIUM NITRATE (UNII: 8M4L3H2ZVZ)  
METHYL SALICYLATE (UNII: LAV5U5022Y)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83522-001-011 in 1 CARTON09/10/2023
1120 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01209/10/2023
Labeler - Medic -33, Inc. (116663992)

Revised: 1/2024
Document Id: 043cadde-b9e2-7c77-e063-6394a90abee6
Set id: 2b64c6c1-c01b-4462-a759-655df564de62
Version: 1
Effective Time: 20240108
 
Medic -33, Inc.