IDO Isopropyl Alcohol Pad by IDO PHARM IDO SWAB A Alcohol Swab

IDO Isopropyl Alcohol Pad by

Drug Labeling and Warnings

IDO Isopropyl Alcohol Pad by is a Otc medication manufactured, distributed, or labeled by IDO PHARM. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

IDO ISOPROPYL ALCOHOL PAD- isopropyl alcohol swab 
IDO PHARM

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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IDO SWAB A Alcohol Swab

Active Ingredient

Isopropyl Alcohol 70%

Purpose

Antiseptic

Uses

• for preparation of the skin prior to an injection
• to decrease bacteria on skin without soap and water

Warnings

​ For external use only.

Flammable. Keep away from heat or flame.

Do not use

• in eyes. In case of contact with eyes, rinse eyes thoroughly with water
• on irritated skin

Stop use and ask a doctor if

• skin irritation or redness develops
• condition persists for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• tear open packet and remove swab (pad)
• apply to skin as needed to clean intended area
• apply to cut, scrape or burn and discard after single use

Other information

• avoid freezing and excessive heat above 104°F (40°C)
• store at room temperature

Inactive ingredients

Purified Water

Package Label - Principal Display Panel

Antiseptic Alcohol Swab

IDO SWAB A

Isopropyl Alcohol 70%

Multi-purpose (Prep/Clean)

For External Use Only

1 Single Use Swab

1.2 in x 1.4 in (3 cm x 3.5 cm)

IDO ISOPROPYL ALCOHOL PAD 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77039-001
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 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77039-001-10	100 in 1 CARTON	07/01/2020	12/24/2021
1		1 in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/01/2020	12/24/2021

Labeler - IDO PHARM (694853523)

Establishment
Name	Address	ID/FEI	Business Operations
IDO PHARM		694853523	manufacture(77039-001)

Revised: 12/2021

Document Id: d3e5f9ca-1c66-754a-e053-2a95a90a488e

34390-5

Set id: aa18319f-64eb-6baf-e053-2995a90a0172

Version: 2

Effective Time: 20211224