ISO BLU 50 PERCENT- isopropyl alcohol liquid

Iso Blu by

Drug Labeling and Warnings

Iso Blu by is a Otc medication manufactured, distributed, or labeled by P & L Development, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (by volume)

Isopropyl alcohol (50% conc)

Purpose

first aid antiseptic

Uses

• first aid to help prevent the risk of infection in minor cuts, scrapes and burns

Warnings

For external use only.

• flammable, keep away from fire or flame
• if taken internally serious gastric disturbances will result

Ask a doctor before use if you have

• deep or puncture wounds, animal bites or 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 one week unless directed by a doctor

Stop use and ask a doctor if

• condition persists or gets worse

Keep out of reach of children.

In case of ingestion, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Directions

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

Other information

• store at room temperature
• does not contain, nor is intended as a substitute for grain or ethyl alcohol

Inactive ingredients

camphor, eucalyptus, FD&C blue #1, glycerin, menthol, purified water

Principal Display Panel

50% Iso-Blu®

Topical Analgesic

Isopropyl Alcohol

Menthol

Eucalyptus

Camphor

Fast temporary pain relief for

aches

soreness

strains

Warning: Flammable, keep away from spark, heat or flame

Manufactured by: PL Developments

1874 Hwy 72 W

clinton, SC 29325

Questions or comments?

Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

FL OZ (mL)

TAMPER EVIDENT: DO NOT USE IF THE UNDER CAP PRINTED SAFETY FOIL IS BROKEN OR MISSING.

Package Label

%0 Percent Iso-Blu

INGREDIENTS AND APPEARANCE

ISO BLU  50 PERCENT
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49580-0269
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
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
EUCALYPTUS CAMALDULENSIS LEAF OIL (UNII: SN6D1J15I6)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GLYCERIN (UNII: PDC6A3C0OX)
MENTHOL (UNII: L7T10EIP3A)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49580-0269-6	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/31/2015	12/30/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333A	05/31/2015	12/30/2021

Labeler - P & L Development, LLC (101896231)