HAND SANITIZER LEMONGRASS- isopropyl alcohol liquid

Hand Sanitizer Lemongrass by

Drug Labeling and Warnings

Hand Sanitizer Lemongrass 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 use
on 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 in your palm and rub hands together briskly until dry.

Inactive ingredients

Aloe vera extract, Carbomer, Lemongrass Essential Oil, Aminomethyl Propanol, Water.

Questions?
Contact Pacific Refill Club at
+1 877-770-7590 Mon-Fri 9am - 4pm PST.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

HAND SANITIZER LEMONGRASS 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79883-001
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
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WEST INDIAN LEMONGRASS OIL (UNII: 5BIA40E9ED)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79883-001-01	120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020
2	NDC: 79883-001-02	250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020
3	NDC: 79883-001-03	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2020
4	NDC: 79883-001-04	90 mL in 1 TUBE; Type 0: Not a Combination Product	07/01/2020
5	NDC: 79883-001-05	1000 mL in 1 BOTTLE; 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(79883-001)