ISOPROPYL RUBBING ALCOHOL 70 PERCENT- isopropyl alcohol liquid

Isopropyl Rubbing Alcohol 70 Percent by

Drug Labeling and Warnings

Isopropyl Rubbing Alcohol 70 Percent by is a Otc medication manufactured, distributed, or labeled by Pharma Nobis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Isopropyl Alcohol 70% by volume

Purpose

First aid antiseptic

Use

First aid to help prevent the risk of infection in.

• minor cuts
  
• scrapes
  
• burns

Warnings

For external use only.

• Flammable, keep way from spark, heat and flame.

Ask a doctor before use for

• deep wounds
  
• animal bites
  
• serious burns

When using this product

• do not get into eyes
  
• do not apply over large areas of the body
  
• do not use longer than 1 week

Stop use and ask a doctor if

condition persists or gets worse

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

• clean the affected area.
  
• apply a small amount of this product on the affected area 1 to 3 times daily.
  
• may be covered with sterile bandage.
  
• if bandaged, let it dry first.

Other Information

• store at room temperature
  
• does not contain, nor is intended as a substitute for grain or ethyl alcohol.
  
• will produce serious gastric disturbances if taken internally.

Inactive Ingredient

purified water

Good Neighbor Label

Health Mart Label

Sunmark Label

INGREDIENTS AND APPEARANCE

ISOPROPYL RUBBING ALCOHOL 70 PERCENT 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82645-913
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	700 mg  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82645-913-16	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016
2	NDC: 82645-913-32	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016
3	NDC: 82645-913-28	3800 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	01/01/2016

Labeler - Pharma Nobis, LLC (118564114)

Registrant - Pharma Nobis, LLC (118564114)

Establishment
Name	Address	ID/FEI	Business Operations
Pharma Nobis, LLC		118564114	manufacture(82645-913) , analysis(82645-913) , pack(82645-913) , label(82645-913)