ALTRA NON-ALCOHOL FOAMING HAND SANITIZER WITH ALLANTOIN AND ALOE- benzalkonium chloride solution 
Buckeye International, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active ingredient

Benzalkonium Chloride 0.12%

Purpose

Antibacterial

Uses

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

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

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)

container label

ALTRA NON-ALCOHOL FOAMING HAND SANITIZER WITH ALLANTOIN AND ALOE 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30805-015
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.12 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:30805-015-0550 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
2NDC:30805-015-07550 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
3NDC:30805-015-091000 mL in 1 BAG; Type 0: Not a Combination Product04/15/2020
4NDC:30805-015-021250 mL in 1 BAG; Type 0: Not a Combination Product04/15/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/15/2020
Labeler - Buckeye International, Inc. (077132280)
Establishment
NameAddressID/FEIBusiness Operations
Buckeye International, Inc.077132280manufacture(30805-015)

Revised: 4/2020
Document Id: a35ad6ce-700d-5b42-e053-2995a90a7da6
Set id: a35ad6ce-700c-5b42-e053-2995a90a7da6
Version: 1
Effective Time: 20200415
 
Buckeye International, Inc.