Label: HYPERCLN SANITIZING WIPES- anti-microbial wipe cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 78847-320-40 - Packager: Falcon Safety Products, Inc.
- Category: HUMAN OTC DRUG LABEL
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 October 27, 2022
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- Active Ingredient
- Purpose
- Warning
- Ask a doctor
- Keep out of the reach of children.
- Dosage and Administration
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Inactive ingredients
Water, Decyl Glucoside, Glycerin, Sodium hydroxymethylglycinate, Citric Acid, PEG-12 Dimethicone, Fragrance, Sodium Benzoate, Potassium Sorbate, Allantoin, Tocopheryl Acetate, Aloe Barbadensis Leaf Water, Chamomilla Recutita (Matricaria) Flower Water, Panthenol, Tetrasodium EDTA, Benzyl Alcohol, Sodium Hydroxide
- Use
- Primary Displaly Panel
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INGREDIENTS AND APPEARANCE
HYPERCLN SANITIZING WIPES
anti-microbial wipe clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:78847-320 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.0013 g in 1 g Inactive Ingredients Ingredient Name Strength POTASSIUM SORBATE (UNII: 1VPU26JZZ4) CHAMOMILE (UNII: FGL3685T2X) TETRAHYDROLINALOOL (UNII: UM4XS5M134) CITRONITRILE (UNII: MS598KEL3M) EUCALYPTOL (UNII: RV6J6604TK) SODIUM HYDROXYMETHYLGLYCINATE (UNII: DIG6BWZ9XT) ALLANTOIN (UNII: 344S277G0Z) ALOE VERA LEAF (UNII: ZY81Z83H0X) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) PANTHENOL (UNII: WV9CM0O67Z) WATER (UNII: 059QF0KO0R) PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) EDETATE SODIUM (UNII: MP1J8420LU) SODIUM BENZOATE (UNII: OJ245FE5EU) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) GLYCERIN (UNII: PDC6A3C0OX) 3,7-DIMETHYL-1-OCTANOL (UNII: DPY9K1927C) 3,3'-DIHYDROXYDIPROPYL ETHER (UNII: S1OQ81LMNA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:78847-320-40 0.0052 g in 1 PACKAGE; Type 0: Not a Combination Product 07/13/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/13/2020 Labeler - Falcon Safety Products, Inc. (150582500) Registrant - Dan Mor (514523067) Establishment Name Address ID/FEI Business Operations Dan Mor 514523067 manufacture(78847-320)