SANI PROFESSIONAL BRAND SANI-HANDS FOR KIDSHAND WIPES HAND WIPES- benzalkonium chloride cloth

Sani Professional Brand Sani-Hands for KidsHand Wipes by

Drug Labeling and Warnings

Sani Professional Brand Sani-Hands for KidsHand Wipes by is a Otc medication manufactured, distributed, or labeled by Professional Disposables International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Use

For hand washing to decrease bacteria on the skin

Warnings

• For external use only.
• If swallowed, get medical help or contact a Poison Control Center right away.
• Do not use in the eyes.
• Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a physician.

Inactive ingredients

Water, SD Alcohol 40, Sorbic Acid, PPG-2 Hydroxyethyl Cocamide, Disodium EDTA, Aloe Barbadensis Leaf Juice, Fragrance

Active ingredient

Benzalkonium Chloride 0.13% w/w

Purpose

Antiseptic handwash

Keep out of reach of children

Keep this out of reach of children unless under adult supervision.

Directions

-To start feed: Remove cover and discard seal from container. From center of wipe roll, pull up wipe corner; tear off first wipe for use.Twist next wipe into a point and thread through the hole in the container cover. Pull through about one inch. Replace cover. Pull out wipes as needed and snap off at 90o angle. Keep center cap closed to prevent moisture loss.

- Wipe hands, fingers, interdigital areas and wrists thoroughly with towelette. Be sure to utilize the entire wipe surface. Allow to dry.

- For dirty hands, use first wipe to clean hands, then discard wipe; sanitize with second wipe.

- Discard after single use.

Other Information

Lot No. and Expiration Date can be found on canister

Principal Display Panel

Front Canister Label



Back Canister Label

INGREDIENTS AND APPEARANCE

SANI PROFESSIONAL BRAND SANI-HANDS FOR KIDSHAND WIPES  HAND WIPES
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10819-7009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
SORBIC ACID (UNII: X045WJ989B)
PPG-2 HYDROXYETHYL COCAMIDE (UNII: 34N07GUJ3X)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
MICROCITRUS AUSTRALIS FRUIT (UNII: 9DNS80T428)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10819-7009-3	6 in 1 CASE	11/06/2013
1		933 mL in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2013

Labeler - Professional Disposables International, Inc. (800777117)

Establishment
Name	Address	ID/FEI	Business Operations
Professional Disposables International, Inc.		800777117	manufacture(10819-7009)