GRIZZLY CREEK NATURALS HAND SANITIZER- alcohol liquid

Grizzly Creek Naturals Hand Sanitizer by

Drug Labeling and Warnings

Grizzly Creek Naturals Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by BLACK BIRD POTENTIALS INC., GRIZZLY CREEK FARMS, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

Active ingredient Isopropyl Alcohol 99%

Purpose Antiseptic

DRUG FACTS

Active ingredient Isopropyl Alcohol 99%

Purpose Antiseptic

Uses

To decrease bacteria on the skin that could

cause disease; Recommended for repeated use

Warnings

● For external use only: hands ● Flammable, keep away from fire or flame ● When using this product keep out of eyes. In

case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest

Stop use and ask a doctor if

Stop use and ask a doctor if irritation and redness develop or condition persists for more than 72 hours

Keep out of reach of children

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

Directions

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult super-vision. Use of product not recommended for infants.

Other information

Do not store above 105ºF. May discolor some fabrics. Harmful to wood finishes and plastics.

Inactive ingredients

water, fragrance, aloe vera juice, sodium benzoate, potassium sorbate, xanthan gum.

Directions

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult super-vision. Use of product not recommended for infants.

Uses

To decrease bacteria on the skin that could cause disease; Recommended for repeated use

PRINCIPAL DISPLAY PANEL

30 mL NDC: 73816-101- 01

INGREDIENTS AND APPEARANCE

GRIZZLY CREEK NATURALS HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73816-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE ARBORESCENS LEAF (UNII: 09TD8L5SQV)
XANTHAN GUM (UNII: TTV12P4NEE)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
VACCINIUM MYRTILLUS ANTHOCYANOSIDES (UNII: R911H793SU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73816-101-01	30 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	03/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/31/2020

Labeler - BLACK BIRD POTENTIALS INC. (116959113)

Registrant - BLACK BIRD POTENTIALS INC. (116959113)

Establishment
Name	Address	ID/FEI	Business Operations
GRIZZLY CREEK FARMS, LLC		043551953	manufacture(73816-101)