ALTRA NON-ALCOHOL FOAMING HAND SANITIZER WITH ALLANTOIN AND ALOE- benzalkonium chloride solution

Altra Non-Alcohol Foaming Hand Sanitizer with Allantoin and Aloe by

Drug Labeling and Warnings

Altra Non-Alcohol Foaming Hand Sanitizer with Allantoin and Aloe by is a Otc medication manufactured, distributed, or labeled by Buckeye International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride 0.12%

Purpose

Antibacterial

Uses

• Hand sanitizer to help reduce bacteria on the skin that could cause disease
• Recommended for repeated use

Warnings

For external use only.

When using this product do not use in or near eyes.

If in eyes, flush thoroughly with water.

If irritation or rash appears and persists, stop use and see a physician.

Keep out of reach of children.

If swallowed, call a physician or Poison Control Center immediately.

Directions

• Dispense an adequate amount of hand sanitizer
• Rub hads together until completely dry

Inactive ingredients

Water (Aqua), Cocamidopropyl Betaine, Lauramine Oxide, Tetrasodium EDTA, Allantoin, Fragrance (Parfum), Aloe Barbadensis Leaf Juice, Methylchloroisothiazolinone, Methylisothiazolinone

Questions?

Call Buckeye International, Inc. 314-291-1900

Monday through Friday 8:00 a.m. to 5:00 p.m. CST

PRINCIPAL DISPLAY PANEL

ALTRA

Non-Alcohol

Foaming hand

Sanitizer

with Allantoin and Aloe

Hand Hygiene

Manufactured by

Buckeye International

2700 Wagner Place Maryland Heights

MO 63043 USA (314) 291-1900

Product # 71151120

Net Contents 1250 mL (42.2 fl oz)

INGREDIENTS AND APPEARANCE

ALTRA NON-ALCOHOL FOAMING HAND SANITIZER WITH ALLANTOIN AND ALOE 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 30805-015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.12 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALLANTOIN (UNII: 344S277G0Z)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
WATER (UNII: 059QF0KO0R)
EDETATE SODIUM (UNII: MP1J8420LU)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 30805-015-05	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/15/2020
2	NDC: 30805-015-07	550 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/15/2020
3	NDC: 30805-015-09	1000 mL in 1 BAG; Type 0: Not a Combination Product	04/15/2020
4	NDC: 30805-015-02	1250 mL in 1 BAG; Type 0: Not a Combination Product	04/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/15/2020

Labeler - Buckeye International, Inc. (077132280)

Establishment
Name	Address	ID/FEI	Business Operations
Buckeye International, Inc.		077132280	manufacture(30805-015)