SANINTA ANTISEPTIC WIPE- alcohol liquid

Saninta Antiseptic Wipe by

Drug Labeling and Warnings

Saninta Antiseptic Wipe by is a Otc medication manufactured, distributed, or labeled by LL Pharma, LL Pharma Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Isopropyl alcohol 70% v/v

Purpose

Antiseptic

Use

Antiseptic wipe to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame.

Do not use

Do not use

• In children less than 2 months of age
• On open skin wounds

When using this product

When using this product Keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Directions

• Wipe hands thoroughly and carefully for at least 30 seconds. Allow to dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

• Store between 15ºC - 30ºC (59º-86ºF)
• Avoid freezing and excessive heat above 40ºC (104ºF).

Inactive ingredients

Purified Water USP

Questions or Comments?

Questions or Comments? Tel.: 1-833-336-6159

Package Label - Principal Display Panel

NDC: 81351-001-01

Product: 001-01

Effective for hand sanitizing

For personal hand hygiene to help prevent the spread of bacteria

Saninta

Antiseptic Wipe

Antiseptic Alcohol Wipe

Isopropyl Alcohol 70% USP

51 Unit large wipes

8" x 4 3/4 " wipes

Manufactured by:

LL Pharma Inc.

5789 rue Cypihot, Saint-Laurent (Montreal), Quebec H4S 1R3

Made in Canada

www.llpharmainc.com

LOT #:

EXP.:

F001

VER. 01

RE: 01-2021

INGREDIENTS AND APPEARANCE

SANINTA ANTISEPTIC WIPE 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81351-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 L  in 1 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81351-001-01	51 in 1 BOX	03/09/2021
1		0.0027 L in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	03/09/2021

Labeler - LL Pharma (206925146)

Registrant - LL Pharma (206925146)

Establishment
Name	Address	ID/FEI	Business Operations
LL Pharma Inc.		206925146	manufacture(81351-001) , analysis(81351-001) , label(81351-001) , pack(81351-001)