HAND SANITIZER FRESH EVERGREEN- isopropyl alcohol spray

Hand Sanitizer FRESH EVERGREEN by

Drug Labeling and Warnings

Hand Sanitizer FRESH EVERGREEN by is a Otc medication manufactured, distributed, or labeled by TAICORP ENTERPRISES LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Isopropyl alcohol 70% v/v

Purpose

Antiseptic

Use

To help reduce bacteria on the skin.

Warnings

• For external use only.
• Flammability warning. Keep away from heat or flame.

Do not useon children less than 2 years of age (unless directed by a doctor).

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and consult a doctor if irritation develops.

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

• Dispense enough product in your palm to thoroughly cover your hands.
• Rub hands together briskly until dry.

Inactive ingredients

 Aloe Vera Extract, Bergamot Essential Oil, Fir Needle Essential Oil, Fragrance, Water.

Questions?

Contact Scentuals at +1877-770-7590 Mon-Fri 9am - 4pm PST.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

HAND SANITIZER FRESH EVERGREEN 
isopropyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79883-009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BERGAMOT OIL (UNII: 39W1PKE3JI)
ABIES SIBIRICA LEAF OIL (UNII: XRY0V4VZKZ)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79883-009-01	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020
2	NDC: 79883-009-02	120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020
3	NDC: 79883-009-03	250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020
4	NDC: 79883-009-04	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020
5	NDC: 79883-009-05	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020
6	NDC: 79883-009-06	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/01/2020

Labeler - TAICORP ENTERPRISES LIMITED (202875738)

Establishment
Name	Address	ID/FEI	Business Operations
TAICORP ENTERPRISES LIMITED		202875738	manufacture(79883-009)