Zep Foam San description, usages, side effects, indications, overdosage, supplying and lots more!

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Zep Foam San

Zep, Inc

Alcohol Free Foaming Hand Sanitizer




FULL PRESCRIBING INFORMATION

Benzethonium chloride 0.2%

Antiseptic

  • Kills 99.99% of most common germs that cause illness in as little as 15 seconds.
  • No rinsing required.
  • Does not contain alcohol.
  • Sanitizing to decrease bacteria on skin.

For external use only.

When using this product

  • Avoid eye contact.
  • If in eyes, rinse promptly and thoroughly with water.

Stop use and ask doctor if skin irritation or redness persists for more than 72 hours.

Keep out of reach of children and pets. Children must be supervised in use of this product.

If swallowed, get medical help or contact a Poison Control Center immediately.

  • Press pump to dispense product onto hands.
  • Rub hands together allowing foam to contact all areas, especially around the nails.
  • Continue until foam had disappeared and/or hands are dry.
  • Store at 20 to 25C (68 to 77F).
  • Do not freeze.
  • Dispose in accordance with all applicable federal, state and local regulations.

Water, Glycerin, PEG/PPG-18/18 Dimethicone, DMDM Hydantoin (and) Iodopropynyl Butylcarbomate, Hydroxypropyl Methylcellulose

Call 1-800-I-BUY-ZEP (1-800-428-9937)

Zep Foam San

Zep Foam San

Zep Foam San

Benzethonium Chloride LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:66949-880
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzethonium chloride BENZETHONIUM .02 g

Inactive Ingredients

Ingredient Name Strength
water
GLYCERIN
PEG/PPG-18/18 DIMETHICONE
DMDM HYDANTOIN
IODOPROPYNYL BUTYLCARBAMATE
HYDROXYPROPYL CELLULOSE (TYPE J)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:66949-880-03 550 in 1 BOTTLE, PLASTIC
2 NDC:66949-880-10 1000 in 1 BOTTLE, PLASTIC
3 NDC:66949-880-12 2500 in 1 BOTTLE, PLASTIC
4 NDC:66949-880-50 75708 in 1 PACKAGE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2003-03-18


Zep Non Alcohol Foam Sanitizer

Benzethonium Chloride LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:66949-248
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzethonium chloride BENZETHONIUM .02 g

Inactive Ingredients

Ingredient Name Strength
water
GLYCERIN
PEG/PPG-18/18 DIMETHICONE
DMDM HYDANTOIN
IODOPROPYNYL BUTYLCARBAMATE
HYDROXYPROPYL CELLULOSE (TYPE J)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:66949-248-15 550 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2011-07-14


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Be sure to consult your doctor before taking any medication!
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