Oxymetazoline Hydrochloride
FDA Label NDC 65841-711

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Cadila Healthcare Limited for the product Oxymetazoline Hydrochloride (NDC 65841-711). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, when using this product, other, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Oxymetazoline hydrochloride 0.05%

Purpose

Nasal decongestant

Uses

  • Temporarily relieves nasal congestion due to:

    •                                    ■ a cold ■ hay fever ■ upper respiratory allergies

    • promotes nasal and sinus drainage
    • temporarily relieves sinus congestion and pressure
    • helps clear nasal passages; shrinks swollen membranes

Warnings

Ask a doctor before use if you have

■ heart disease ■ high blood pressure ■ thyroid disease ■ diabetes

■ 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

Other

Stop use and ask a doctor if symptoms persist.

If pregnant or breast-feeding, ask a health professional before use.

Manufactured by:

Cadila Healthcare Ltd.

Ahmedabad, India

Rev.: 00/00

Revision Date: 05/31/2011

Keep Out Of Reach Of Children

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

Directions

  • adults and children 6 to under 12 years of age (with adult supervision):

    • 2 or 3 sprays in each nostril not more 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.

      • Shake well before use. Before using the first time, remove the protective cap from the tip and prime metered pump by depressing firmly several times. To spray, hold bottle with thumb at base and nozzle between first and second fingers. Without tilting head, insert nozzle into nostril. Fully depress pump all the way down with a firm even stroke and sniff deeply. Wipe nozzle clean after use.

Other Information

  • Store between 20° - 25°C (68° - 77°F)
  • retain carton for future reference on full labeling

Inactive Ingredients

benzalkonium chloride solution, camphor, edetate disodium, eucalyptol, glycin, menthol, polyethylene glycol, polysorbate 80, propylene glycol, purified water, sodium chloride, sodium hydroxide.

Container And Carton Labels

NDC 65841-711-07

Oxymetazoline Hydrochloride Concentrated Vapor Nasal Spray, ¾ FL OZ (22 mL)

Rx only

Zydus

Oxymetazoline HCl Nasal Spray, 3/4 Fl Oz (22 mL)-image1 (Oxymetazolinehcl Figure 01)

Oxymetazoline HCl Nasal Spray, 3/4 Fl Oz (22 mL)-image1 (Oxymetazolinehcl Figure 01)

Oxymetazoline HCl Nasal Spray, 3/4 Fl Oz (22 mL)-image2 (Oxymetazolinehcl Figure 02)

Oxymetazoline HCl Nasal Spray, 3/4 Fl Oz (22 mL)-image2 (Oxymetazolinehcl Figure 02)

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