esika description, usages, side effects, indications, overdosage, supplying and lots more!

esika

Ventura Corporation Ltd.

  • 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
ésika total sec NEUTRAL FRAGRANCE Alcohol Free Unisex Deodorant and Antiperspirant - All day protection

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active Ingredient

Aluminum Chlorohydrate 4.5%

Purpose

Antiperspirant

Uses

  • Reduces underarm perspiration.
  • All day protection.

Warnings

For external use only

Do not use on broken skin

Ask a doctor before use if you have kidney disease

Stop use and ask a doctor if rash or irritation occurs

When using this product

  • Keep away from face and mouth to avoid breathing it.
  • Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120 deg. F.
  • Use only as directed. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Apply to underarms only.

Inactive ingredients

BUTANE, ISOBUTANE, PROPANE, CYCLOPENTASILOXANE, C12-15 ALKYL BENZOATE, DISTEARDIMONIUM HECTORITE, ALUMINUM STARCH OCTENYLSUCCINATE, PARFUM (FRAGRANCE), BISABOLOL, TRICLOSAN, PROPYLENE GLYCOL, AQUA (WATER), BAMBUSA ARUNDINACEA LEAF EXTRACT.

P.R.: Distributed by Ventura Corporation, Ltd., San Juan, Puerto Rico 00926.

PRINCIPAL DISPLAY PANEL - 125 mL Bottle Label

ésika

total
sec

NEUTRAL FRAGRANCE

Alcohol Free
Unisex
Deodorant and
Antiperspirant
All day protection

24
hours

125 ml e (4.2 fl.oz.)

PRINCIPAL DISPLAY PANEL - 125 mL Bottle Label

esika

Aluminum Chlorohydrate SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:13537-506
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALUMINUM CHLOROHYDRATE ALUMINUM CHLOROHYDRATE 0.045 g

Inactive Ingredients

Ingredient Name Strength
BUTANE
isobutane
propane
CYCLOMETHICONE 5
ALKYL (C12-15) BENZOATE
DISTEARDIMONIUM HECTORITE
ALUMINUM STARCH OCTENYLSUCCINATE
LEVOMENOL
TRICLOSAN
propylene glycol
water
BAMBUSA BAMBOS LEAF

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:13537-506-01 125 in 1 BOTTLE, SPRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part350 2013-05-27


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