ALCOHOL PREP PADS- 70%isopropyl alcohol swab

Alcohol Prep Pads by

Drug Labeling and Warnings

Alcohol Prep Pads by is a Otc medication manufactured, distributed, or labeled by Raya Pharmaceuticals LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

For the preparation of the skin prior to an injection

Wipe injection site vigorously and discard

PRECAUTIONS

- For external use only
- Flammable, keep away from fire or flame

WARNINGS AND PRECAUTIONS

Warnings

· For external use only
· Flammable, keep away from fire or flame

Stop Use

· If irritation and redness develop.
· If the condition persists consult your health care practitioner.

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

STORAGE AND HANDLING

Store at room temperature

Protect from freezing. Avoid excessive heat.

Dosage and Administration

Wipe injection site vigorously and discard

WARNINGS

For External Use

Flamable, Keep Away from fire and flame

Inactive ingredients

Water

Keep out of reach of children

Keep out of reach of children, if swallowed get medical help or contact a poison center right away.

Purpose section

Use for preperation of the skin prioir to an injection

Isopropyl Alcohol 70%........................Purpose: Antiseptic

Active ingredients

Isopropyl Alcohol 70%........................Antiseptic

PRINCIPAL DISPLAY PANEL

ALCOHOL PREP PAD

Saturated with 70% Isopropyl Alcohol

100 Swabs

For External use only

INGREDIENTS AND APPEARANCE

ALCOHOL PREP PADS 
70%isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82098-814
Route of Administration	TOPICAL

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

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82098-814-10	0.7 mL in 1 POUCH; Type 0: Not a Combination Product	03/12/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	03/12/2022

Labeler - Raya Pharmaceuticals LLC (106631637)