Active Ingredient

Isopropyl Alcohol 70%

Purpose

Antiseptic

Use(s)

• First aid to help prevent infection in minor cuts, scrapes, and burns

• For preparation of the skin prior to an injection

Warnings

For External Use only

Flammable. Keep away from fire or flame.

Do not use

• In the eyes or over large areas of the body

• Longer than 1 week unless directed by a doctor

• With electrocautery procedures

Ask a doctor before use if you have

Deep or puncture wounds, animal bites, or serious burns.

Stop use and ask a doctor if

Condition persists for more than 72 hours or gets worse.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

• When used for first aid: Clean the affected area. Apply a small amount of this product on the area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let dry first.

• When used to prepare an injection site: Apply product to the injection site prior to injection.

Other Information

Store at room temperature
Avoid excessive heat

Inactive Ingredient

Water

Label

1113-1116 Box Master

Label 1113-50

1113-50_BX_MASTER 1113-50

Label 1113UB-24

1113UB-2 BX_MASTER 1113UB-24

Label 1113UB-10

1113UB-10_BX_MASTER 1113UB-10

ALCOHOL PREP
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:67777-121
Route of Administration	TOPICAL

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

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

Product Characteristics
Color		Score
Shape	RECTANGLE	Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:67777-121-20	20000 in 1 CASE	07/01/2010
1	NDC:67777-121-19	100 in 1 BOX
1	NDC:67777-121-14	0.55 mL in 1 POUCH; Type 0: Not a Combination Product
2	NDC:67777-121-18	1000 in 1 CASE	07/01/2010
2	NDC:67777-121-17	100 in 1 BOX
2	NDC:67777-121-16	0.7 mL in 1 POUCH; Type 0: Not a Combination Product
3	NDC:67777-121-12	2000 in 1 CASE	07/01/2010
3	NDC:67777-121-11	200 in 1 BOX
3	NDC:67777-121-13	0.55 mL in 1 POUCH; Type 0: Not a Combination Product
4	NDC:67777-121-26	1000 in 1 CASE	07/01/2010
4	NDC:67777-121-27	50 in 1 BOX
4		0.55 mL in 1 POUCH; Type 0: Not a Combination Product
5	NDC:67777-121-22	480 in 1 CASE	07/01/2010
5	NDC:67777-121-21	24 in 1 BOX
5		0.55 mL in 1 POUCH; Type 0: Not a Combination Product
6	NDC:67777-121-24	1000 in 1 CASE	07/01/2010
6	NDC:67777-121-23	10 in 1 BOX
6		0.55 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M003	07/01/2010

Labeler - Dynarex Corporation (008124539)

1113, 1114, 1116, 1113UB-24, 1113UB-10, 1113-50 Sterile Alcohol Prep Pads