Label: NGA ALCOHOL WIPES SANDSTONE- ethanol swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated October 5, 2023

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  • SPL UNCLASSIFIED SECTION

    Hand sanitizer (65%(w/w) denatured ethanol in an aqueous solution):

    - Manufactured using United States Pharmacopoeia (USP) grade ingredients including USP water.

    - The alcohol (ethanol) is (USP or Food Chemical Codex (FCC) grade), and is denatured according to Alcohol & Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.

  • ACTIVE INGREDIENT

    Ethanol Alcohol 65%

    Antiseptic

    USES

    Uses: Reducing Bacteria on skin

  • WARNINGS

    Flammable. Keep away from fire and flame. External use only. Do not use in eyes. If contact occurs, flush thoroughly with water. Stop use and ask doctor if redness or irritation develops and continues for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact the poison control centre immediately.

    Keep out of reach of children.

  • Directions

    How to Use: insert pack into case, remove sticker. Dispense one wipe. WIpe hands thoroughly including between fingers & around fingerails. Allow to air dry.

    Dispense one wipe. Wipe hands thoroughly including between fingers & around fingernails. Allow to Air dry.

  • Other Information

    Store below 104°F(40°C). Each wipe is 15 x 12 cm. May discolour certain fabrics. Do not use as a baby wipe, on the face, or in the intimate area. Made in UK for Never Go Alone Ltd.

  • INACTIVE INGREDIENT

    AQUA, ALOE VERA EXTRACT (ALOE BARDANENSIS WATER), GLYCERIN, CERAMIDE 2, GREEN TEA LEAF EXTRACT, CALENDULA, CHAMOMILE, GINSENG EXTRACT, FRAGRANCE (PARFUM)

  • PRINCIPAL DISPLAY PANEL

    10 wipes; 83732-0110-1 10 Wipes - SANDSTONE PACKET

  • INGREDIENTS AND APPEARANCE
    NGA ALCOHOL WIPES SANDSTONE 
    ethanol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83732-0110
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL17.55 g  in 27 g
    Inactive Ingredients
    Ingredient NameStrength
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) 0.02 g  in 27 g
    ASIAN GINSENG (UNII: CUQ3A77YXI) 0.01 g  in 27 g
    GREEN TEA LEAF (UNII: W2ZU1RY8B0) 0.02 g  in 27 g
    GLYCERIN (UNII: PDC6A3C0OX) 0.3 g  in 27 g
    WATER (UNII: 059QF0KO0R) 8.21 g  in 27 g
    PALMITOYL MYRISTYL SERINATE (UNII: 203U03P988) 0.02 g  in 27 g
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.6 g  in 27 g
    CHAMOMILE (UNII: FGL3685T2X) 0.01 g  in 27 g
    FRAGRANCE 13576 (UNII: 5EM498GW35) 0.26 g  in 27 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83732-0110-127 g in 1 PACKET; Type 0: Not a Combination Product10/05/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/05/2023
    Labeler - NEVER GO ALONE (225874426)
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