SYMMETRY 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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Drug Facts

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 hands 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 8:00to 5:00 p.m. CST

For General Hand Sanitizing

Symmetry

Non-Alcohol Foaming

Hand Sanitizer

w/ Allantoin and Aloe

Product # 90153000

Net Content  1000  ml (33.8 fl oz)

container label

SYMMETRY NON-ALCOHOL FOAMING HAND SANITIZER WITH ALLANTOIN AND ALOE  
benzalkonium chloride solution
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:30805-010
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
Water (UNII: 059QF0KO0R)  
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
EDETATE SODIUM (UNII: MP1J8420LU)  
Allantoin (UNII: 344S277G0Z)  
Aloe Vera Leaf (UNII: ZY81Z83H0X)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
Methylisothiazolinone (UNII: 229D0E1QFA)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:30805-010-02 1250 mL in 1 BAG; Type 0: Not a Combination Product 11/01/2011
2 NDC:30805-010-05 50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/01/2011
3 NDC:30805-010-07 550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/01/2011
4 NDC:30805-010-09 1000 mL in 1 BAG; Type 0: Not a Combination Product 04/07/2014
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 11/01/2011
Labeler - Buckeye International, Inc. (077132280)
Establishment
Name Address ID/FEI Business Operations
Buckeye International, Inc. 077132280 manufacture(30805-010)

Revised: 12/2016
Document Id: 39935c6b-8456-4166-ba1e-b18b4a79383c
Set id: 2750f62c-e650-428a-b070-5c13ff8e378e
Version: 2
Effective Time: 20161227
 
Buckeye International, Inc.