ANTISEPTIC DISINFECTANT- silsesquioxane liquid

ANTISEPTIC DISINFECTANT by

Drug Labeling and Warnings

ANTISEPTIC DISINFECTANT by is a Otc medication manufactured, distributed, or labeled by Nano Care Deutschland AG. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

The liquid guard is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

ACTIVE INGREDIENT

Silsesquioxane 2.9 % v/v. Purpose: Liquid Guard AntiSeptic

Antiseptic

Antiseptic

INDICATIONS & USAGE

Liquid Guard Antiseptic to help reduce bacteria that potentially can cause disease.

WARNINGS

For external use only. Keep out of reach of eyes, ears, and mouth

DO NOT USE

Keep out of reach of children’s

WHEN USING

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 if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

STOP USE

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.

DOSAGE & ADMINISTRATION

Place enough product to clean the infected area. Do not use of wet surfaces / skin.

STORAGE AND HANDLING

Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

purified water USP

Maximum 1000000000 mL in 1 CONTAINER (

79836-510-01)

5000 mL NDC: 79836-510-01

INGREDIENTS AND APPEARANCE

ANTISEPTIC DISINFECTANT 
silsesquioxane liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79836-510
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	0.56 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	98.7 mL  in 100 mL
METHYL ALCOHOL (UNII: Y4S76JWI15)	0.5 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79836-510-01	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/28/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/28/2020

Labeler - Nano Care Deutschland AG (314463865)

Registrant - Nano Care Deutschland AG (314463865)

Establishment
Name	Address	ID/FEI	Business Operations
Nano Care Deutschland AG		314463865	manufacture(79836-510)