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

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

Drug Labeling and Warnings

Symmetry 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

Active ingredient

Benzalkonium Chloride 0.12%

PURPOSE

Purpose

Antibacterial

INDICATIONS & USAGE

Uses

Hand sanitizer to help reduce bacteria on the skin that could cause disease

Recommended for repeated use

WARNINGS

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.

DOSAGE & ADMINISTRATION

Directions

Dispense an adequate amount of hand sanitizer

Rub hands together until completely dry

INACTIVE INGREDIENT

Inactive ingredients

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

QUESTIONS

Questions?

Call: Buckeye International, Inc. 314-291-1900

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

PRINCIPAL DISPLAY PANEL

For General Hand Sanitizing

Symmetry

Non-Alcohol Foaming

Hand Sanitizer

w/ Allantoin and Aloe

Product # 90153000

Net Content  1000  ml (33.8 fl oz)

INGREDIENTS AND APPEARANCE

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)