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

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Zylast Antiseptic

Bocchi Laboratories Inc.




FULL PRESCRIBING INFORMATION

Ethyl alcohol 76%

Antiseptic

  • Handwash to decrease bacteria on the skin that potentially can cause disease.
  • Recommended for repeated use.
  • For external use only.
  • Flammable. Keep away from flame.
  • Discontinue use if irritation and redness develops. Consult a doctor if condition persists for more than 72 hours.  

If swallowed, immediately call Poison Control Center or doctor.

  • Wet hands thoroughly with product and allow to dry without wiping.
  • Store at 20-25°C (68-77°F)

Water, Polyaminopropyl Biguanide, Panthenol, Hydroxyethyl Ethylcellulose, Farnesol, PEG- 12 Dimethicone, Benzethonium Chloride. 

Ethyl alcohol 76%

Antiseptic

  • Handwash to decrease bacteria on the skin that potentially can cause disease.
  • Recommended for repeated use.
  • For external use only.
  • Flammable, keep away from flame.
  • Avoid contact with eyes. In case of eye contact, rinse eyes thoroughly with water.
  • Discontinue use if irritation and redness develops. Consult a doctor if condition persists for more than 72 hours.
  • If swallowed, immediately call Poison Control Center or doctor.
  • Wet hands thoroughly with product and allow to dry without wiping.
  •  Store at 20-25°C (68-77°F)

Water, Polyaminopropyl Biguanide, Panthenol, Hydroxyethyl Ethylcellulose, Farnesol, PEG- 12 Dimethicone, Benzethonium Chloride. 

NDC 57702-464-00
Zylast
Broad Spectrum
Antimicrobial
Antiseptic
2 fl oz/ 59.1 mL

Zylast Antiseptic

NDC 57702-464-03
Zylast
Broad Spectrum
Antimicrobial
Antiseptic
8 fl oz 236.6 mL

Zylast Antiseptic

NDC 57702-464-13
Zylast
Broad Spectrum
Antimicrobial
Antiseptic
1000mL (33.8oz)

Zylast Antiseptic

Zylast Antiseptic

Ethyl Alcohol LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57702-464
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALCOHOL ALCOHOL 0.76 mL

Inactive Ingredients

Ingredient Name Strength
Farnesol
water
POLIHEXANIDE
PANTHENOL
benzethonium chloride

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57702-464-00 59.1 in 1 BOTTLE
2 NDC:57702-464-03 236.6 in 1 BOTTLE
3 NDC:57702-464-13 1000 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2011-06-01


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