BODYOGRAPHYPRO ANTI-BACTERIAL SANITIZING- ethyl alcohol spray

BODYOGRAPHYPRO ANTI-BACTERIAL SANITIZING by

Drug Labeling and Warnings

BODYOGRAPHYPRO ANTI-BACTERIAL SANITIZING by is a Otc medication manufactured, distributed, or labeled by Robanda International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

ETHANOL (Alcohol Denat.) 60.00%

Purpose

Antimicrobial

uses

Works instantly to effectively eliminate germs and bacteria from cosmetic products, tester displays, makeup kits, workstations or hands

Warnings

Flammable. Keep away from fire or flame.
Do not use in or near the eyes, in case of contact, rinse thoroughly with water.
For external use only. Stop use and ask a doctor if irritation or rash appears and lasts. Avoid contact with broken skin.

If swallowed, seek medical help immediately.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Directions

• Hold spray 6” away from products, hands and surfaces, gently spray once or twice from one side to the other, in a swiping motion.

OTHER INFORMATION

• Store between 15-30C (56-86F)
• Avoid freezing and excessive heat about 40C (104F)

Inactive ingredients

Water (aqua), Citrullus lanatus (Watermelon) Fruit Extract, Chenopodium quinoa Extract, Urea, Sucrose, Glycerin, Sodium Lactate, Sodium
PCA, Phenoxyethanol, Ethylhexylglycerin, Caprylyl Glycol, Hexylene Glycol, Fragrance

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BODYOGRAPHYPRO ANTI-BACTERIAL SANITIZING 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53950-6010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	60 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
WATER (UNII: 059QF0KO0R)
WATERMELON (UNII: 231473QB6R)
CHENOPODIUM QUINOA SEED (UNII: OO4K72NZ2X)
UREA (UNII: 8W8T17847W)
SUCROSE (UNII: C151H8M554)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM LACTATE (UNII: TU7HW0W0QT)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53950-6010-1	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M014	08/15/2020

Labeler - Robanda International, Inc. (048214287)