INDUSTRIAL SANITIZING- benzethonium chloride and dimethicone lotion

Industrial Sanitizing by

Drug Labeling and Warnings

Industrial Sanitizing by is a Otc medication manufactured, distributed, or labeled by R&R Lotion, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active Ingredients	Purpose
Benzethonium Chloride 0.2%	Antibacterial
Dimethicone 2.0%	Skin Protectant

Uses

Skin protectant, temporarily protects against harmful Pathogens & Stimuli while killing 99.99% of Germs for up to Four Hours.

Warnings

For external use only

• When using this product, aviod contact with eyes
• In case of eye contact, flush with water

• Keep out of reach of children, except under adult supervision
• If swallowed, get medical help
• Discontinue use if skin irritation or redness develops.

Directions

Rub into hands and body until absorbed.

Ingredients

DI Water, Incroquat TMS, Propylene Glycol, Sunflower Butter, Octyl Palmitate, Stearyl Alcohol, Cetyl Alcohol, Geoguard Ultra, Aloe Vera, Jojoba, Blue Agave, Blueberry, Cranberry, Pomegranate, Raspberry, Strawberry, Green Tea, Green Coffee Bean, Grape Seed, Acai Berry, Vitamins A, D, & E

Questions or Comments?

Call (480) 443-9255

PRINCIPAL DISPLAY PANEL - 118 ML Bottle Label

HAND LOTION

STRENGTH

INDUSTRIAL
HAND SANITIZER

FOUR HOUR
PROTECTION

4 FL. OZ. (118ML) e

INGREDIENTS AND APPEARANCE

INDUSTRIAL SANITIZING 
benzethonium chloride and dimethicone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59555-902
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzethonium Chloride (UNII: PH41D05744) (Benzethonium - UNII:1VU15B70BP)	Benzethonium Chloride	2 mg  in 1 mL
Dimethicone (UNII: 92RU3N3Y1O) (Dimethicone - UNII:92RU3N3Y1O)	Dimethicone	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Propylene Glycol (UNII: 6DC9Q167V3)
Stearyl Alcohol (UNII: 2KR89I4H1Y)
cholecalciferol (UNII: 1C6V77QF41)
Cetyl Alcohol (UNII: 936JST6JCN)
vitamin A (UNII: 81G40H8B0T)
Behentrimonium Methosulfate (UNII: 5SHP745C61)
Cetostearyl Alcohol (UNII: 2DMT128M1S)
.Alpha.-Tocopherol (UNII: H4N855PNZ1)
Ethylhexyl Palmitate (UNII: 2865993309)
Gluconolactone (UNII: WQ29KQ9POT)
Sodium Benzoate (UNII: OJ245FE5EU)
Calcium Gluconate (UNII: SQE6VB453K)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59555-902-08	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2	NDC: 59555-902-04	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3	NDC: 59555-902-10	946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
4	NDC: 59555-902-11	3785 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
5	NDC: 59555-902-13	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
6	NDC: 59555-902-07	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333A	12/21/2015

Labeler - R&R Lotion, Inc. (062979000)