RX200 Foaming Instant Hand Sanitizer description, usages, side effects, indications, overdosage, supplying and lots more!

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RX200 Foaming Instant Hand Sanitizer

The Bullen Companies, Inc.
Kutol Products Company, Inc.

RX200 Foaming Instant Hand Sanitizer


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

RX200 Foaming Instant Hand Sanitizer Uses

Products 17 & 78: For handwashing to decrease bacteria on skin.

Product 41: Hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Purpose

Products 17 & 78: Antibacterial Agent

Product 41: Antibacterial Handwashing

Active Ingredient

Benzalkonium Chloride 0.13% w/w

Warnings

Products 17 & 41: For external use only. Avoid contact with eyes. If contact occurs, flush with water. Stop use and ask a doctor if, in rare instances, redness or irritations develops. If condition persists for more than 72 hours, consult a physician. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center.

Product 78: For external use only. Do not use in the eyes. In rare instances of redness or irritation, discontinue use. If condition persists for more than 72 hours, consult a physician. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center.

Inactive Ingredients

Water, Propylene Glycol, Cocamidopropyl Betaine, Aloe Barbadensis Leaf, Tocopheryl Acetate (Vitamin E), PEG-7 Glyceryl Cocoate, Fragrance, Phenoxyethanol, Tetrasodium EDTA.

Directions

To decrease bacteria on skin, apply a small amount to palm. Briskly rub covering hands with product until dry.

Warnings

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

RX200 Foaming Instant Hand Sanitizer

RX200 Foaming Instant Hand Sanitizer

RX200 Foaming Instant Hand Sanitizer

RX200 Foaming Instant Hand Sanitizer

Benzalkonium Chloride LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57356-207
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 4.918 g

Inactive Ingredients

Ingredient Name Strength
COCAMIDOPROPYL BETAINE
water
PEG-7 GLYCERYL COCOATE
propylene glycol
PHENOXYETHANOL
MONOSODIUM ETHYLENEDIAMINETETRAACETATE
Aloe Vera Leaf
.ALPHA.-TOCOPHEROL ACETATE, DL-

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57356-207-17 50 in 1 BOTTLE, PUMP
2 NDC:57356-207-41 1000 in 1 POUCH
3 NDC:57356-207-78 950 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 2009-12-14


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