Drug Labeling and Warnings

Drug Details


ISOPROPYL ALCOHOL- isopropyl alcohol swab 
Becton Dickinson and Company

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.


Drug Facts

Active Ingredient

Isopropyl Alcohol, 70% v/v




for the preparation of skin prior to an injection to decrease germs in minor cuts and scrapes.


  • For External use only.

Keep out of the reach of children.

If swallowed, get medical help or contact a poison control center immediately.

Caution do not apply to irritated skin.

Do not use in the eyes, or on mucous membranes.

In case of deep or puncture wounds, consult a doctor.


wipe injection site vigorously.

Other Information

store at room temperature.

Inactive Ingredient


Principal Display Panel – Carton Label.

NDC/HRI# 08290-3268-95


100 Swabs

BD Alcohol Swabs

Antiseptic for preparation of the skin prior to injection

CALL: 1.888.BDCARES (1.888.232.2737)

VISIT: www.bd.com/us/diabetes

WRITE: BD, 1 Becton Drive, Franklin Lakes, NJ 07417

Principal Display Panel – Carton Label
isopropyl alcohol swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 8290-3268
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Isopropyl Alcohol (UNII: ND2M416302) (Isopropyl Alcohol - UNII:ND2M416302) Isopropyl Alcohol0.75 g
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 8290-3268-9512 in 1 CARTON10/01/1993
1100 in 1 BOX
11 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A10/01/1993
Labeler - Becton Dickinson and Company (001292192)

Revised: 4/2013
Becton Dickinson and Company

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