Benzoin Compound Tincture description, usages, side effects, indications, overdosage, supplying and lots more!

Benzoin Compound Tincture

Humco Holding Group, Inc.

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Humco Benzoin Compound Tincture, USP

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active Ingredient

Benzoin

Purpose

Pral mucosal protectant

Use

Forms a coating over wound for protecting recurring canker sores

Warnings

For expternal use only. Do not swallow. Do not exceed recommended dosage.

When using this product

Children under 12 years of age should be supervised in the use of this product.

Do not use for more than 7 days unless directed by a dentist or doctor.

Stop use and consult a dentist or doctor if

sore mouth symptoms do not improve in 7 days. irritation, pain or redness persists or worsens. swelling, rash or fever develops.

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

Adults and children 6 months of age and older: Dry the affected area, with cotton swab, apply undiluted to the affected area not more often than every 2 hours.

Children under 6 months of age: Consult a dentiest or doctor.

Other information

Flammable: Keep away from spark, heat or flame.

Inactive Ingredients

Alcohol 77%, Aloe, Storax, Tolu Balsam

Principal Display Panel - 16oz

Principal Display Panel - 16oz

Principal Display Panel - 2 oz

Principal Display Panel - 2 oz

Benzoin Compound Tincture

Benzoin Resin LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0395-0243
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BENZOIN RESIN 1000 mg

Inactive Ingredients

Ingredient Name Strength
ALCOHOL
ALOE
TOLU BALSAM

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0395-0243-16 473 in 1 BOTTLE, PLASTIC
2 NDC:0395-0243-92 59 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part356 2008-01-01


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