FIRST AID ONLY ALCOHOL ANTISEPTIC PAD- alcohol pad swab
Acme United Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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First Aid Only Alcohol Antiseptic Pad

Active Ingredients

Active Ingredients Isopropyl Alcohol 70%

Purpose

Antispetic Cleanser

Uses

Uses •For preparation of the skin prior to 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

Stop Use if irritation or redness develop.If condition persists consult your health care practicioner.

Keep out of reach of children

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

Directions

Directions •Wipe Injection site vigorously and discard.

Inactive Ingredients

Inactive Ingredients purified water

Package Label Principal Display Panel

Carton Label Package Label

FIRST AID ONLY ALCOHOL ANTISEPTIC PAD
alcohol pad swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0924-0009(NDC:71310-200)
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 g in 100 g

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

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:0924-0009-00	1 g in 1 PACKET; Type 0: Not a Combination Product	07/26/2017
2	NDC:0924-0009-01	100 in 1 CARTON	06/28/2018
2		1 g in 1 PACKET; Type 0: Not a Combination Product
3	NDC:0924-0009-02	200 in 1 CARTON	06/28/2018
3		1 g in 1 PACKET; Type 0: Not a Combination Product
4	NDC:0924-0009-03	10 in 1 CARTON	01/22/2019
4		1 g in 1 PACKET; Type 0: Not a Combination Product
5	NDC:0924-0009-04	20 in 1 CARTON	01/22/2019
5		1 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	07/26/2017

Labeler - Acme United Corporation (001180207)

Name	Address	ID/FEI	Business Operations
Establishment
Acme United Corporation		045924339	relabel(0924-0009) , repack(0924-0009)

Name	Address	ID/FEI	Business Operations
Establishment
Acme United Corporation		080119599	repack(0924-0009) , relabel(0924-0009)