Fresh Protect Skin Sanitizer description, usages, side effects, indications, overdosage, supplying and lots more!

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Fresh Protect Skin Sanitizer

Omega Tech Labs Inc.

Fresh Protect Skin Sanitizer Foam




FULL PRESCRIBING INFORMATION

DRUG FACTS

Benzalkonium chloride 0.1%

Antiseptic

For hand sanitizing. To decrease bacteria on the skin.

For external use only.

in the eyes. In case of eye contact, rinse eyes thoroughly with water.

if irritation or redness develops, or if condition persists more than 72 hours.

Instruct children on proper use. If swallowed, get medical help or contact a Poison Control Center right away.

Apply a small amount on your hands. Rub hands together until dry. When hands are visibly soiled, wash with soap and water.

Water, Aloe Barbadensis Leaf Extract, Glycerin, Citrus Grandis (Grapefruit) Seed Extract, Thymus Vulgaris (Thyme) Extract, Camellia Sinensis Leaf (Green Tea) Extract, Avena Sativa (Oat) Extract, Peppermint Essential Oil, Polysorbate 20, Potassium Sorbate, Sodium Benzoate.

Fresh Protect
99.9% Natural
Skin Sanitizer Foam
Kills 99.99% of Germs
No Alcohol
7.5 fl. oz. (222 ml)

Fresh Protect Skin Sanitizer

Fresh Protect Skin Sanitizer

Benzalkonium Chloride LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:20802-1501
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 0.001 g

Inactive Ingredients

Ingredient Name Strength
water
Aloe Vera Leaf
GLYCERIN
Pummelo
THYMUS VULGARIS LEAF
GREEN TEA LEAF
AVENA SATIVA LEAF
PEPPERMINT OIL
POLYSORBATE 20
POTASSIUM SORBATE
SODIUM BENZOATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:20802-1501-1 50 in 1 BOTTLE
2 NDC:20802-1501-2 222 in 1 BOTTLE
3 NDC:20802-1501-3 800 in 1 BAG

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 2010-12-16


Fresh Protect Skin Sanitizer

Benzalkonium Chloride LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:20802-1503
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 0.001 g

Inactive Ingredients

Ingredient Name Strength
water
Aloe Vera Leaf
GLYCERIN
Pummelo
THYMUS VULGARIS LEAF
GREEN TEA LEAF
AVENA SATIVA LEAF
PEPPERMINT OIL
POLYSORBATE 20
POTASSIUM SORBATE
SODIUM BENZOATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:20802-1503-1 3785 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 2010-12-16


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Be sure to consult your doctor before taking any medication!
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