FIRST AID ONLY ALCOHOL ANTISEPTIC PAD- isopropyl alcohol swab

First Aid Only Alcohol Antiseptic Pad by

Drug Labeling and Warnings

First Aid Only Alcohol Antiseptic Pad by is a Otc medication manufactured, distributed, or labeled by Acme United Coporation, Acme United Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active Ingredient

Isopropyl Alcohol, 70%

PURPOSE

Purpose

Antiseptic Cleanser

INDICATIONS & USAGE

Use for preparation of the skin prior to an injection

WARNINGS

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

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 and 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 Store at room temperature 15 ο​​ - 30 ο C (59 ο - 86 ο F)

INACTIVE INGREDIENT

Inactive Ingredient purified water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FIRST AID ONLY ALCOHOL ANTISEPTIC PAD 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0924-0015(NDC:59647-500)
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: 0924-0015-01	10 in 1 CARTON	03/06/2020
1		1 mL in 1 POUCH; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
2	NDC: 0924-0015-00	1 mL in 1 PACKET; Type 0: Not a Combination Product	03/06/2020
3	NDC: 0924-0015-02	20 in 1 CARTON	03/06/2020
3		1 mL in 1 POUCH; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
4	NDC: 0924-0015-03	100 in 1 CARTON	03/06/2020
4		1 mL in 1 POUCH; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
5	NDC: 0924-0015-04	200 in 1 CARTON	03/06/2020
5		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	03/06/2020

Labeler - Acme United Coporation (001180207)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		045924339	relabel(0924-0015) , repack(0924-0015)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		080119599	relabel(0924-0015) , repack(0924-0015)