Label: W.SKIN TREEMON TONER (melaleuca alternifolia- tea tree extract liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 74997-0023-1 - Packager: J&J COMPANY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated May 8, 2021
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Water, Butylene Glycol, Glycerin, Melaleuca Alternifolia (Tea Tree) Extract, Rosa Damascena Flower Water, Centella Asiatica Extract, Panthenol, Asiaticoside, Madecassoside, Fructan, Mentha Rotundifolia Leaf Extract, Hamamelis Virginiana (Witch Hazel) Leaf Extract, Melissa Officinalis Leaf Extract, Cymbopogon Schoenanthus Extract, Vaccinium Angustifolium (Blueberry) Fruit Extract, Rubus Idaeus (Raspberry) Fruit Extract, Rosa Centifolia Flower Water, Portulaca Oleracea Extract, Scutellaria Baicalensis Root Extract , Paeonia Lactiflora Root Extract, Lonicera Japonica (Honeysuckle) Flower Extract, Betaine, Sodium Hyaluronate, Xanthan Gum, Propanediol, 1,2-Hexanediol, Hydroxyacetophenone, Ethylhexylglycerin, Disodium EDTA
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
W.SKIN TREEMON TONER
melaleuca alternifolia (tea tree) extract liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74997-0023 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K) (MELALEUCA ALTERNIFOLIA LEAF - UNII:G43C57162K) MELALEUCA ALTERNIFOLIA LEAF 1 g in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74997-0023-1 300 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/08/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/08/2021 Labeler - J&J COMPANY (688995236) Registrant - J&J COMPANY (688995236) Establishment Name Address ID/FEI Business Operations J&J COMPANY 688995236 manufacture(74997-0023) , label(74997-0023) , pack(74997-0023)