SANIGO RUBBING ALCOHOL- rubbing alcohol liquid

Sanigo Rubbing Alcohol by

Drug Labeling and Warnings

Sanigo Rubbing Alcohol by is a Otc medication manufactured, distributed, or labeled by KPaul, Kpaul. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Isopropyl Alcohol 70% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Rubbing Alcohol

Use

First aid to help prevent the risk of infection in minor cuts, scrapes, and burns.

Warnings

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

Do not use

• in children less than 2 months of age
• with electrocautery procedures
• on open skin wounds
• longer than 1 week unless directed by a doctor
• over large areas of the body

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

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.

Directions

• Clean the affacted area
• Apply a small amount of this product 1 to 3 times daily.
• May be covered with a sterile bandage. If bandaged, let dry first.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

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

Inactive ingredients

purified water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SANIGO RUBBING ALCOHOL 
rubbing alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77979-200
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	30 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77979-200-01	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
2	NDC: 77979-200-10	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
3	NDC: 77979-200-50	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
4	NDC: 77979-200-16	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
5	NDC: 77979-200-08	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
6	NDC: 77979-200-04	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
7	NDC: 77979-200-80	80 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
8	NDC: 77979-200-60	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020

Labeler - KPaul (785308797)

Registrant - Kpaul (785308797)

Establishment
Name	Address	ID/FEI	Business Operations
KPaul		785308797	manufacture(77979-200) , label(77979-200)