NATURAL HAND SANITIZER- alcohol gel

NATURAL HAND SANITIZER by

Drug Labeling and Warnings

NATURAL HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by TUBBY TODD, Health Specialty. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

DENATURED DEHYDRATED ALCOHOL 40B  62.5%

PURPOSE

ANTISEPTIC

USES

For hand washing to decrease bacteria on skin.

WARNINGS

For external use only. Flammable. Keep away from sources of fire or flame.
When using this product Do not use near eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if skin irritation develops.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, seek medical advice or contact a Poison Control Center immediately.

DIRECTIONS

• Apply onto palm of hand.
• Cover hands with product by thoroughly rubbing and allow to air dry without wiping.Use undiluted.
• Supervise children under 6 years
• Not recommended for infants

OTHER INFORMATION

• Store below 86°F / 30°C
• Keep out of direct sunlight.

INACTIVE INGREDIENT

WATER, GLYCERIN, PROPYLENE GLYCOL, CARBOMER, PROPANEDIOL 2-AMINO METHYL-1 PROPANOL SOLUTION. ALOE BARBADENSIS LEAF JUICE, TOCOPHERYL ACETATE (VITAMIN E ACETATE), HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, VACCINIUM MACROCARPON (CRANBERRY) FRUIT EXTRACT, PUNICA GRANATUM EXTRACT, VACCINIUM ANGUSTIFOLIA (BLUEBERRY) EXTRACT, FRAGARIA VESCA (STRAWBERRY) FRUIT EXTRACT, ACTINIDIA CHINENSIS (KIWI) EXTRACT

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NATURAL HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73088-201
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
PROPANEDIOL (UNII: 5965N8W85T)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
SUNFLOWER OIL (UNII: 3W1JG795YI)
CRANBERRY (UNII: 0MVO31Q3QS)
POMEGRANATE (UNII: 56687D1Z4D)
BLUEBERRY (UNII: 253RUG1X1A)
STRAWBERRY (UNII: 4J2TY8Y81V)
KIWI FRUIT (UNII: 71ES77LGJC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73088-201-11	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/21/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/21/2019

Labeler - TUBBY TODD (052545299)

Establishment
Name	Address	ID/FEI	Business Operations
Health Specialty		794053863	manufacture(73088-201)