Label: ALCOHOL PREP PAD - MEDIUM- isopropyl alcohol swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 Label Information

Updated August 24, 2016

If you are a consumer or patient please visit this version.

View All Sections
  • Active Ingredients

    Isopropyl Alcohol 70%

  • Purpose

    Antiseptic

  • Use

    For preparation of the skin prior to injection.

  • Warnings

    • For external use only.
    • Flammable, keep away from fire or flame.

    Do Not Use

    • with electrocautery procedures.
    • In the eyes. If contact occurs, flush eyes with water.

    Stop Use

    If irritation and redness develop. If condition continues, consult your health care practitione.

    Keep out of reach of children.

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

  • Directions

    • Wipe injection area and discard.
  • Other information

    Store at room temperature 15 oC~30 oC(59 oF~86 oF)

  • Inactive Ingredients

    purified water

  • SPL UNCLASSIFIED SECTION

    Shanghai Yinjing Medical Supplies Co., Ltd.
    No.586 Yuanxi RD.Nanhui Industry Park,
    Shanghai 201300
    Tel:+86-21-68016633  Http://www.yinjing.cn
    E-mail: zhl@yinjing.cn
    Made in China
    LOT:                          EXP:

  • PRINCIPAL DISPLAY PANEL

    inin
    NDC:44019-111-01

    1 pad/pouch

    ALCOHOL PREP PAD
    Saturated with 70% Isopropyl Alcohol

    For External Use Only

  • Product Label

    Alcohol prep pad medium

  • INGREDIENTS AND APPEARANCE
    ALCOHOL PREP PAD - MEDIUM  
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44019-111
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:44019-111-011 in 1 POUCH08/03/2016
    10.45 g in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/03/2016
    Labeler - Yinjing Medical Technology (Shanghai) Co., Ltd. (530501535)
    Registrant - Yinjing Medical Technology (Shanghai) Co., Ltd. (530501535)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!