Label: NU SKIN EPOCH- alcohol gel

  • NDC Code(s): 12488-1800-1
  • Packager: Alberto-Culver USA Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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 December 14, 2009

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

  • Active Ingredient

    SD Alcohol 40-B (62%)

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  • Usage

    Disinfects and provides protection by killing 99.99% of the most common harmful germs and bacteria.

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  • Warnings

    For external use only. Keep out of reach of children. Keep out of eyes. Discontinue use if irritation develops. If condition persists for more than 72 hours consult a physician. Flammable, keep away from fire or flame.

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  • Directions

    Place a teaspoon of product in one hand. Spread on both hands, applying liberally. Rub gently until dry.

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  • Inactive Ingredients

    Water (Aqua), Lavandula Angustifolia (Lavender) Oil, Lonicera Japonica (Honeysuckle) Flower Extract, PEG-40 Hydrogenated Castor Oil, Carbomer, Aminomethyl Propanol, Fragrance (Parfum), Chlorphenesin.

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  • Questions?

    1-888-742-7626

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  • SPL UNCLASSIFIED SECTION

    Mfd. in the U.S.A exclusively for
    NSE Products, Inc., Provo, UT 84601

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  • PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label

    epoch®

    with Lavender,
    Honeysuckle Extract,
    and Chlorphenesin

    Antiseptic

    Hand Sanitizer

    100 ml e (3.4 fl. oz.)

    PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label (Front)
    PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label (Back)
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  • INGREDIENTS AND APPEARANCE
    NU SKIN EPOCH 
    alcohol gel
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:12488-1800
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol 61.9937 mL  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    Water (UNII: 059QF0KO0R)  
    Polyoxyl 40 Hydrogenated Castor Oil (UNII: 7YC686GQ8F)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:12488-1800-1 100 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH FINAL part333 06/01/2009
    Labeler - Alberto-Culver USA Inc. (021679448)
    Establishment
    Name Address ID/FEI Business Operations
    Alberto-Culver USA Inc. 021679448 ANALYSIS, MANUFACTURE
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