Dryses Antiperspirant Solution description, usages, side effects, indications, overdosage, supplying and lots more!

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Dryses Antiperspirant Solution

SESVALIA USA LLC.

DRYSES Antiperspirant Solution


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient

Aluminum Chlorohydrate 20%

Purpose

Antiperspirant

Use

  • Reduces underarm sweat

Warnings

For external use only.

Flammable, keep away from fire or flame

Ask a doctor before use

if you have kidney disease.

Do not use

  • on broken skin
  • on irritated or recently shaved skin

When using this product

  • avoid contact with eyes.
  • in case of eye contact, flush eyes with water
  • temporary itching sensation may occur.

Stop use and ask a doctor if

rash or irritation occurs.

Keep out of reach of children

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

Directions

• apply to underarms only

• use your fingertips or cotton ball to apply the product.

• during first week of use, product may be applied each evening. 

• after the first week, apply product once or twice at night.

• before applying product, dry area to avoid irritation.

Inactive Ingredients

Alcohol Denat, Butylparabean, Ethylparaben, Isobutylparaben, Methylparaben, Phenoxyethanol, Propylene Glycol, Propylparaben, Water.

DRYSES Antiperspirant Solution 3.4 fl oz (100ml) (63181-0015-1)

SesdermaDRYSES

Aluminium Chlorohydrate

Antiperspirant Solution

Reduces underarm

perspiration

Developed for sportsmen

All skin types

3.4 fl oz (100ml)

Sesderma

Manufactured by

SESDERMA S.L.

Pol. Industrial

Rafelbunol. C/ Massamagrell, 5,

46138 Rafelbunol. Valencia (Spain)

Customar service: 902 100 223

Distributed by

SESVALIA USA LLC. 67, Miracle

Mile, Coral Gables, FL 33134 USA

Customer line: (1) 8OO 796 0996

www.sesderma.com

Made in SPAIN

Dryses Antiperspirant Solution

Dryses Antiperspirant Solution

ALUMINUM CHLOROHYDRATE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:63181-0015
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALUMINUM CHLOROHYDRATE ALUMINUM CHLOROHYDRATE 200 mg

Inactive Ingredients

Ingredient Name Strength
BUTYLPARABEN
ETHYLPARABEN
isobutylparaben
METHYLPARABEN
PHENOXYETHANOL
propylene glycol
PROPYLPARABEN
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63181-0015-1 100 in 1 BOTTLE, WITH APPLICATOR

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part350 2014-04-02


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