Supress A

Supress A
SPL v1
SPL
SPL Set ID 410c19f7-213d-cd99-e063-6294a90af5a3
Route
ORAL
Published
Effective Date 2012-08-01
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Dexbrompheniramine (1 mg) Phenylephrine (5 mg) Dextromethorphan (10 mg)
Inactive Ingredients
Glycerin Methylparaben Citric Acid Propylene Glycol Sodium Citrate Sucralose Propylparaben Water Polysorbate 20

Identifiers & Packaging

Marketing Status
OTC MONOGRAPH DRUG Active Since 2012-08-01

Description

Active Ingredient Section DEXBROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE

Purpose

Purpose Section: Antihistamine, Cough suppressant, Nasal descongestant


Medication Information

Purpose

Purpose Section: Antihistamine, Cough suppressant, Nasal descongestant

Description

Active Ingredient Section DEXBROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE

Purpose Section

Purpose Section:

Antihistamine, Cough suppressant, Nasal descongestant

Warning Section

Warning Section:

Keep out of reach of children. In case of overdose,, get medical help or contact Poison Control Center right away.

Question Section

Question Section:

Call weekdays from 8 am to 4 pm AST at 1.787.767.2072

Do Not Use Section

Do not use section:

Do not use more than 6 doses in any 24-hour period, repeat every 4 hour, measure with the dosage device provided.

Do not use with any other device, children 6 to under 12 years of ageL 1 ml, Children under 6 year of age, consult a doctor.

Active Ingredient Section

Active Ingredient Section

DEXBROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE

Inactive Ingredient Section

Inactive Ingredient Section:

citric Acid, flavor, glycerin, methylparaben, polysorbate, propylene glycol, propylparaben, purified water, sodium citrate, sucralose.

Indication and Usage Section

Indication and usage Section:

Use temporarity relieves these symptoms due to hay fever or other upper respiratory allergies:

  • sneezing
  • itchy nose or throat
  • runny nose
  • itchy, watery eyes
  • nasal congestion
  • temporarily controls cough due to minor throat and bronchial irritation associated with inhaled irritants
  • temporarily restores freer breathin througt nose.

Dosage & Administration Section

Dosage & Administration Section:

Do not use more than 6 doses in any 24-hour period, repeat every 4 hour, measure with the dosage device provided.

Do not use with any other device

children 6 to under 12 years of ageL 1 ml, Children under 6 year of age, consult a doctor.

Keep Out of Reach of Children Section

Keep out of reach of children section:

In case of accidental overdose, get medical help or contacta Poison Control Center right away.

Package Label. Principal Display Panel

Package Label. Principal Display Panel

NDC 52083--057-01

SUPRESS A

  • Antihistamine
  • Cough Suppressant
  • Nasal Descongestant

PEDIATRIC DROPS

Sugar, Dye and Alcohol Free

PSEUDOEPHEDRINE & PPA FREE

Net content: 30ml (1Fl, Oz)

Kramer Novis


Structured Label Content

Purpose Section

Purpose Section:

Antihistamine, Cough suppressant, Nasal descongestant

Warning Section

Warning Section:

Keep out of reach of children. In case of overdose,, get medical help or contact Poison Control Center right away.

Question Section

Question Section:

Call weekdays from 8 am to 4 pm AST at 1.787.767.2072

Do Not Use Section (Do not use section)

Do not use section:

Do not use more than 6 doses in any 24-hour period, repeat every 4 hour, measure with the dosage device provided.

Do not use with any other device, children 6 to under 12 years of ageL 1 ml, Children under 6 year of age, consult a doctor.

Active Ingredient Section

Active Ingredient Section

DEXBROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE

Inactive Ingredient Section

Inactive Ingredient Section:

citric Acid, flavor, glycerin, methylparaben, polysorbate, propylene glycol, propylparaben, purified water, sodium citrate, sucralose.

Indication and Usage Section (Indication and usage Section)

Indication and usage Section:

Use temporarity relieves these symptoms due to hay fever or other upper respiratory allergies:

  • sneezing
  • itchy nose or throat
  • runny nose
  • itchy, watery eyes
  • nasal congestion
  • temporarily controls cough due to minor throat and bronchial irritation associated with inhaled irritants
  • temporarily restores freer breathin througt nose.

Dosage & Administration Section

Dosage & Administration Section:

Do not use more than 6 doses in any 24-hour period, repeat every 4 hour, measure with the dosage device provided.

Do not use with any other device

children 6 to under 12 years of ageL 1 ml, Children under 6 year of age, consult a doctor.

Keep Out of Reach of Children Section (Keep out of reach of children section)

Keep out of reach of children section:

In case of accidental overdose, get medical help or contacta Poison Control Center right away.

Package Label. Principal Display Panel

Package Label. Principal Display Panel

NDC 52083--057-01

SUPRESS A

  • Antihistamine
  • Cough Suppressant
  • Nasal Descongestant

PEDIATRIC DROPS

Sugar, Dye and Alcohol Free

PSEUDOEPHEDRINE & PPA FREE

Net content: 30ml (1Fl, Oz)

Kramer Novis


Advanced Ingredient Data


Raw Label Data

All Sections (JSON)