MED-NAP STERILE ALCOHOL PREP PADS- isopropyl alcohol swab

Med-Nap Sterile Alcohol Prep Pads by

Drug Labeling and Warnings

Med-Nap Sterile Alcohol Prep Pads by is a Otc medication manufactured, distributed, or labeled by Acme United Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredient

Isopropyl Alcohol 70% v/v

PURPOSE

Purpose

Antiseptic Cleanser

INDICATIONS & USAGE

Use For preparation of the skin prior to an injection

DO NOT USE

Do Not Use ● with electrocautery procedures ● In the eyes. If contact occurs, flush

eyes with water

STOP USE

Slop Use If irritation or redness develop. If condition persists consult your health care practitioner.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed get medical help or consult a Poison

Control Center right away.

DOSAGE & ADMINISTRATION

Directions ● Wipe injection site vigorously and discard.

OTHER SAFETY INFORMATION

Other Information Sterile unless pouch is opened or damaged. Store at room temperature 15 ο​​ - 30 ο C (59 ο - 86 ο F)

INACTIVE INGREDIENT

Inactive Ingredient purified water

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

QUESTIONS

Questions 800-835-2263

PRINCIPAL DISPLAY PANEL

Prep Pad Box

INGREDIENTS AND APPEARANCE

MED-NAP STERILE ALCOHOL PREP PADS 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0924-0500
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: 0924-0500-01	200 in 1 BOX	07/12/2021
1		1 mL in 1 POUCH; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
2	NDC: 0924-0500-00	1 mL in 1 POUCH; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug	07/12/2021
3	NDC: 0924-0500-02	50 in 1 BOX	07/12/2022
3		1 mL in 1 POUCH; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
4	NDC: 0924-0500-04	100 in 1 BOX	07/12/2022
4		1 mL in 1 POUCH; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/12/2021

Labeler - Acme United Corporation (001180207)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		045924339	label(0924-0500) , pack(0924-0500)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		080119599	label(0924-0500) , pack(0924-0500)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		117825595	manufacture(0924-0500)