GFS BIOPROTECT HAND SANITIZER ALOE VERA -- benzalkonium chloride spray

GFS BIOPROTECT HAND SANITIZER ALOE VERA by

Drug Labeling and Warnings

GFS BIOPROTECT HAND SANITIZER ALOE VERA by is a Otc medication manufactured, distributed, or labeled by GFS US LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DESCRIPTION

BioProtect Hand Sanitizer contains 0.13% antiseptic agent Benzalkonium Chloride formulated with  Water,1-Ocatadecanaminium, N-N-dimethyl-N-[3-(trimethoxysilyl)propyl]-,chloride, C12-C15 Pareth-3, Polyaminopropyl biguanide, Caprylyl glucoside, Citronellol, Sorbic Acid, Glycerin, Aloe Barbadensis (Aloe) Leaf Extract, and  D and C Green No.5. It is alcohol-free, non-toxic and kills 99.99% of germs.

ACTIVE INGREDIENT

Benzalkonium Chloride 0.13%.............................................Antiseptic

PURPOSE

• Antispetic

INDICATIONS & USAGE

• Hand sanitizer to help decrease bacteria on skin

• Recommended for repeated use

WARNINGS

• For external use only

• Do not use in ears or mouth

KEEP OUT OF REACH OF CHILDREN

• Keep out of reach on children

• Children must be supervised in use of this product

DOSAGE & ADMINISTRATION

• Apply a small amount into your palm and thoroughly spread on both hands
• Rub into skin until dry
  

GENERAL PRECAUTIONS

• Review MSDS before handling the product

WHEN USING

• When using this product do not use in ears or mouth

• Avoid contact with eyes
• In case of eye contact, rinse eyes thoroughly with water

STOP USE

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

INACTIVE INGREDIENT

• Water,1-Ocatadecanaminium, N-N-dimethyl-N-[3-(trimethoxysilyl)propyl]-,chloride, C12-C15 Pareth-3, Polyaminopropyl biguanide, Caprylyl glucoside, Citronellol, Sorbic Acid, Glycerin, Aloe Barbadensis (Aloe) Leaf Extract, and  D and C Green No.5

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GFS BIOPROTECT HAND SANITIZER ALOE VERA  -
benzalkonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76426-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y)	Benzalkonium Chloride	0.0013 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
DIMETHYLOCTADECYL(3-(TRIMETHOXYSILYL)PROPYL)AMMONIUM CHLORIDE (UNII: IQ36O85WQ4)
C12-15 PARETH-12 (UNII: 131316X18L)
POLYAMINOPROPYL BIGUANIDE (UNII: 322U039GMF)
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)
.BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)
SORBIC ACID (UNII: X045WJ989B)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
D&C Green No. 5 (UNII: 8J6RDU8L9X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76426-011-01	11 g in 1 BOTTLE, SPRAY
2	NDC: 76426-011-02	28 g in 1 BOTTLE, SPRAY
3	NDC: 76426-011-03	55 g in 1 BOTTLE, SPRAY
4	NDC: 76426-011-04	110 g in 1 BOTTLE, SPRAY
5	NDC: 76426-011-05	225 g in 1 BOTTLE, SPRAY
6	NDC: 76426-011-06	1000 g in 1 BOTTLE
7	NDC: 76426-011-07	3790 g in 1 BOTTLE
8	NDC: 76426-011-08	204300 g in 1 DRUM
9	NDC: 76426-011-09	2204600 g in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
10	NDC: 76426-011-10	800 g in 1 BAG
11	NDC: 76426-011-11	1200 g in 1 BAG
12	NDC: 76426-011-12	1800 g in 1 BAG

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/20/2011

Labeler - GFS US LLC (967789228)