Label: NORO-X FOAMING HANDSOAP- o-cymen-5-ol soap
- NDC Code(s): 77935-505-01
- Packager: BIO3S Co.,Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated February 21, 2023
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- Active ingredients
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Inactive ingredients
Water, Disodium Laureth Sulfosuccinate, Glycerin, Cocamidopropyl Betaine, Disodium Cocoamphodiacetate, Lauryl Glucoside,
Sodium Chloride, Capiylyi Glycol, Ethyihexylglycerin, Menthol, Fragrance, Allantoin, Sodium Benzoate, Citric Acid, Bacillus/Canavalia Ensiformis Seed Ferment Extract, Disodium EDTA, Hexylene Glycol, Butylene Glycol, Chrysanthellum Indicum Extract,
RhusSemialata Gall Extract, Propolis Extract, Pinus Densiflora Leaf Extract, Scutellaria Baicalensis Root Extract - Display Panel
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INGREDIENTS AND APPEARANCE
NORO-X FOAMING HANDSOAP
o-cymen-5-ol soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77935-505 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength O-CYMEN-5-OL (UNII: H41B6Q1I9L) (O-CYMEN-5-OL - UNII:H41B6Q1I9L) O-CYMEN-5-OL 0.095 g in 100 mL Inactive Ingredients Ingredient Name Strength DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) SODIUM BENZOATE (UNII: OJ245FE5EU) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) CHRYSANTHELLUM INDICUM TOP (UNII: STJ856D1Z0) MENTHOL (UNII: L7T10EIP3A) ALLANTOIN (UNII: 344S277G0Z) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CAPRYLYL GLYCOL (UNII: 00YIU5438U) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PINUS DENSIFLORA LEAF (UNII: Q1Q9P50WIY) HEXYLENE GLYCOL (UNII: KEH0A3F75J) FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) PROPOLIS WAX (UNII: 6Y8XYV2NOF) SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) RHUS CHINENSIS GALL (UNII: 4W3Y2V7J3R) CANAVALIA ENSIFORMIS WHOLE (UNII: U485ST9OUN) SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77935-505-01 250 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/27/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/27/2022 Labeler - BIO3S Co.,Ltd. (694813103) Registrant - BIO3S Co.,Ltd. (694813103) Establishment Name Address ID/FEI Business Operations BIO3S Co.,Ltd. 694813103 manufacture(77935-505)