FOREVER HAND SANITIZER HAND SANITIZER- alcohol gel

Forever Hand Sanitizer by

Drug Labeling and Warnings

Forever Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Aloe Vera of America, Inc., Dhaliwal Pharmaceuticals Laboratories,LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

• Active ingredient: Purpose
• Ethyl Alcohol 62%: Antimicrobial

Inactive Ingredients

Water (Aqua)

Aloe Barbadensis Leaf Juice (Stabilized* Aloe Vera Gel)

Honey

Isopropyl Alcohol

Fragrance (Parfum)

Glycerin

Tetrahydroxypropyl

Ethylenediamine

Acrylates/C10-30 Alkyl Acrylate Crosspolymer

Tocopheryl Acetate
Isopropyl Myristate.

Purpose Section

Uses

• hand sanitizer to decrease bacteria on the skin
• recommended for repeated use
  

Warnings

Warnings

Fore external use only.

Flammable. Keep away from fire or flame.

Indications & Usage

• do not use in or near the eyes. If contact occurs, rinse throughly with water.
• avoid contact with broken skin.
  

Stop use and ask a doctor if

Stop use and ask a doctor if

• rash or irritation develops and lasts.
  

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.

Dosage & Administration Directions

Directions

• wet hands thoroughly with product
• briskly rub hands together until dry
• children under 6 years of age should be supervised when using this product
  

Other information

• store at 20 °C to 25 °C (68°F to 77°F) when possible.  Do not store above 40 °C (104° F).
• may discolor certain fabrics
  

Package Label Principal Display Panel

Label

INGREDIENTS AND APPEARANCE

FOREVER HAND SANITIZER  HAND SANITIZER
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11697-318
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	36.58 mL  in 59 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
HONEY (UNII: Y9H1V576FH)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
CYMBOPOGON CITRATUS LEAF (UNII: 06JMS448M5)
GLYCERIN (UNII: PDC6A3C0OX)
EDETOL (UNII: Q4R969U9FR)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11697-318-05	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/16/2010

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/16/2010

Labeler - Aloe Vera of America, Inc. (049049463)

Establishment
Name	Address	ID/FEI	Business Operations
Dhaliwal Pharmaceuticals Laboratories,LLC		116933772	manufacture(11697-318)