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Nazil Ofteno Prescribing Information

Package insert / product label
Generic name: naphazoline hydrochloride
Dosage form: eye drops
Drug class: Ophthalmic antihistamines and decongestants

Medically reviewed by Drugs.com. Last updated on Mar 24, 2023.

DRUG FACTS

DRUG FACTS

Active Ingredient

Naphazoline Hydrochloride 0.02%

Purpose

Redness reliever

Indications and Usage for Nazil Ofteno

  • Relieves redness of the eye due to minor eye irritations

Warnings

For external use only

Do not use

if solution changes color or becomes cloudy

Ask a doctor before use

if you havenarrow angle glaucoma

When using this product

  • Do not touch tip of container to any surface to avoid contamination
  • Replace cap after using
  • Overuse may cause more redness of the eye
  • Puplis may become enlarged temporarily

Stop use and ask a doctor if

  • You feel eye pain
  • Change in vision occur
  • Redness or irritation of the eye lasts
  • Condition worsens
  • Symptoms last for more than 72 hours

Keep out of reach of children

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

Nazil Ofteno Dosage and Administration

Put 1 or 2 drops in the affected eye(s) up to 4 times daily

Storage and Handling

  • Store at room temperature
  • Remove contact lenses before using

Inactive ingredients

benzalkonium chloride (as preservative), boric acid, purified water, sodium borate, sodium chloride

Questions?

Call 1-866-282-8871

www.sophia.com.mx

Principal Display Panel

NDC 57619-300-01

Nazil Ofteno

Redness Reliever Eyedrops

0.5 FL OZ (15mL)

Sterile

Principal Display Panel
NAZIL OFTENO
naphazoline hydrochloride solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57619-300
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Naphazoline Hydrochloride (UNII: MZ1131787D) (Naphazoline - UNII:H231GF11BV) Naphazoline Hydrochloride0.20 mg in 1 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:57619-300-011 in 1 PACKAGE
115 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34904/12/2010
Labeler - LABORATORIOS SOPHIA, S.A. DE C.V. (810143636)
Establishment
NameAddressID/FEIBusiness Operations
LABORATORIOS SOPHIA, S.A. DE C.V.810143636manufacture