PlaneAire Hands sandalwood hand sanitizer lotion

PlanreAire Hands Hand Sanitizer by

Drug Labeling and Warnings

PlanreAire Hands Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by EverywhereAire LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PLANREAIRE HANDS HAND SANITIZER- ethyl alcohol gel 
EverywhereAire LLC

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PlaneAire Hands sandalwood hand sanitizer lotion

Active Ingredient(s)

Alcohol 70% v/v.

Purpose

Antiseptic

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

• on open wounds or near eyes. In case of contact with eyes, rinse thoroughly with water

When using this product keep out of eyes. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use if irritation or rash occurs. If condtion persists for more than 72 hours, consult a doctor.

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

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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, rub hands, and allow to dry without wiping.
• For children under 6 years of age, use only under adult supervision to avoid swallowing
• Not recommended for infants

Other information

• Store between 15-30C (59-86F)
• Do not store above 105F
• Avoid freezing
• may discolor some fabrics
• may be harmful to some wood finishes and plastics

Inactive ingredients

aloe vera, glycerin, green tea extract, polyacrylate crosspolymer-6, safflower seed oil, sandalwood fragrance blend, water

Package Label - Principal Display Panel

60 mL NDC: 80335-109-02

PLANREAIRE HANDS HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80335-109
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF POLYSACCHARIDES (UNII: W21O437517)
SAFFLOWER OIL (UNII: 65UEH262IS)
SANDALWOOD OIL (UNII: X7X01WMQ5F)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80335-109-02	60 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/28/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	12/21/2020	10/22/2021

Labeler - EverywhereAire LLC (117635273)

Registrant - EverywhereAire LLC (117635273)

Revised: 12/2023

Document Id: 0cfb17da-3f81-07c2-e063-6394a90a1af3

34390-5

Set id: b6b4ee13-13f5-0dc6-e053-2995a90a0f50

Version: 5

Effective Time: 20231220