Label: HILLYARD CITRUS FRESH ANTIMICROBIAL FOAMING- chloroxylenol liquid
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NDC Code(s):
76402-408-02,
76402-408-03,
76402-408-06,
76402-408-12, view more76402-408-82
- Packager: Hillyard GMP
- 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 September 3, 2015
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Keep Out of Reach of Children
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Directions
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- Apply cleaner to palm of hand.
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- Lather and scrub hands (including fingers, wrist, and cuticles) vigorously for 60 seconds.
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- Rinse with water until all cleaner is removed from hands.
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- Dry completely (incomplete drying may lead to chapped skin).
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- Children under 6 years of age should be supervised when using this product.
- Inactive Ingredients
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Package/Label Principal Display Panel
Hillyard
Citrus Fresh Antimicrobial
Foaming Hand SoapHIL0040803
affinity
DISPENSING SYSTEMPlace cartridge into dispenser, label facing back, and gently push pump into receiver until it clicks into place.
To remove the cartridge and pump, rotate the green ring clockwise and pull the pump out.
HILLYARD INDUSTRIES
PO Box 909,
St. Joseph, MO
64502-0909 U.S.A.
Telephone: 816-233-1321
www.hillyard.comNET CONTENTS 42.3 FL. OZ. 1.25L
PEEL HERE -
INGREDIENTS AND APPEARANCE
HILLYARD CITRUS FRESH ANTIMICROBIAL FOAMING
chloroxylenol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76402-408 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 0.50 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0) POTASSIUM COCOATE (UNII: F8U72V8ZXP) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) PROPANEDIOL (UNII: 5965N8W85T) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) ALCOHOL (UNII: 3K9958V90M) BENZYL ALCOHOL (UNII: LKG8494WBH) PROPYL ALCOHOL (UNII: 96F264O9SV) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETATE SODIUM (UNII: MP1J8420LU) SODIUM HYDROXYMETHYLGLYCINATE (UNII: DIG6BWZ9XT) MONOETHANOLAMINE (UNII: 5KV86114PT) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) SODIUM HYDROXIDE (UNII: 55X04QC32I) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76402-408-06 3785 mL in 1 JUG; Type 0: Not a Combination Product 09/01/2015 2 NDC:76402-408-03 1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/01/2015 3 NDC:76402-408-02 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/01/2015 4 NDC:76402-408-82 414 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/01/2015 5 NDC:76402-408-12 2000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/01/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 09/01/2015 Labeler - Hillyard GMP (969081483) Establishment Name Address ID/FEI Business Operations Hillyard GMP 969081483 MANUFACTURE(76402-408)