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Rosemary, Chamomile, Melaleuca Alternifolia Leaf, Lavandula Angustifolia Liquid FORMULA Disclaimer

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Rosemary, Chamomile, Melaleuca Alternifolia Leaf, Lavandula Angustifolia Liquid FORMULA Disclaimer ZERO HAND SANITIZER- rosemary, chamomile, melaleuca alternifolia leaf, lavandula angustifolia liquid FORMULA 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. ---------- ACTIVE INGREDIENT Active ingredients: Rosmarinus Officinalis (Rosemary) Leaf Extract 1% Chamomilla Recutita (Matricaria) Flower Extract1% Melaleuca Alternifolia (Tea Tree) Leaf Extract 1% Lavandula Angustifolia (Lavender) Flower Extract 1% INACTIVE INGREDIENT Inactive ingredients: Water, Lavandula Angustifolia (Lavender) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Melaleuca Alternifolia (Tea Tree) Leaf Extract, Scutellaria Baicalensis Root Extract, Rhus Semialata Extract, Terminalia Chebula Fruit Extract, Morus Alba Bark Extract, Zanthoxylum Piperitum Fruit Extract, Pulsatilla Koreana Extract, Usnea Barbata (Lichen) Extract, Butylene Glycol, Boswellia Serrata Extract, Centella Asiatica Extract, Camellia Sinensis Leaf Extract, Actinidia Arguta Fruit Extract, Citrus Paradisi (Grapefruit) Seed Extract, Chamaecyparis Obtusa Water, Flavor PURPOSE Purpose: SANITIZER WARNINGS Warnings: 1.Do not use the product on the following areas: Eyes, mouth, and damaged skin (irritation may occur) 2.If you experience any of the following symptoms, stop using the product immediately and consult a doctor or pharmacist. 1) Hypersensitivity symptoms (e.g. rash, erythema, itching and edema) 2) Skin irritation symptoms 3. Other precautions 1) For external use only. (Do not swallow. If swallowed, vomit and consult a doctor or pharmacist) 2) Avoid contact with eyes. If in contact, wash with clean water and consult a doctor or pharmacist. 3) Do not use sealed bandages, cast bandages or packs as they may cause irritation. 4) Do not use this medicine for anal or vaginal areas or hot packs as it may cause irritation. 5) Use only for the intended purpose. 4.Precautions for storage 1) Keep away from direct sunlight and do not expose the product to heating devices or flame. 2) Keep out of reach of children and go to the hospital immediately if swallowed. 3) After use, close the lid completely to prevent the product from drying or foreign objects from getting inside the container. 4) Storing the product in a different container may cause accidents or deterioration of quality. Therefore, keep the product in its original container. Dust or foreign substances may get on the product while using it. KEEP OUT OF REACH OF CHILDREN Keep out of reach of children and go to the hospital immediately if swallowed. Uses Uses: Disinfection of hands and skin Directions Directions (for Gel type) Take an appropriate amount on your hands and rub thoroughly to dry. Directions (for Spray type) Spray the appropriate amount on your hands and rub thoroughly. PACKAGE LABEL - ZERO Hand Sanitizer 60mL Spray PACKAGE LABEL - ZERO Hand Sanitizer 300mL Gel PACKAGE LABEL - ZERO Hand Sanitizer 300mL Spray ZERO HAND SANITIZER rosemary, chamomile, melaleuca alternifolia leaf, lavandula angustifolia liquid Product Information Product T ype HUMAN OTC DRUG Ite m Code (Source ) NDC:74772-0 10 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength 1.0 g RO SEMARY (UNII: IJ6 7X351P9 ) (ROSEMARY - UNII:IJ6 7X351P9 ) ROSEMARY in 10 0 mL 1.0 g CHAMO MILE (UNII: FGL36 8 5T2X) (CHAMOMILE - UNII:FGL36 8 5T2X) CHAMOMILE in 10 0 mL MELALEUCA ALTERNIFO LIA LEAF (UNII: G43C5716 2K) (MELALEUCA MELALEUCA ALTERNIFOLIA 1.0 g ALTERNIFOLIA LEAF - UNII:G43C5716 2K) LEAF in 10 0 mL LAVANDULA ANGUSTIFO LIA SUBSP. ANGUSTIFO LIA FLO WER (UNII: LAVANDULA ANGUSTIFOLIA 1.0 g 19 AH1RAF4M) (LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER - SUBSP. ANGUSTIFOLIA in 10 0 mL UNII:19 AH1RAF4M) FLOWER Inactive Ingredients Ingredient Name Strength Wa ter (UNII: 0 59 QF0 KO0 R) Butylene Glyco l (UNII: 3XUS8 5K0 RA) Packaging Marketing Start Marketing End # Item Code Package Description Date Date NDC:74772-0 10 - 6 0 mL in 1 BOTTLE, SPRAY; Type 0 : No t a Co mbinatio n 1 0 3/0 1/20 20 0 1 Pro duct NDC:74772-0 10 - 2 30 0 mL in 1 CONTAINER; Type 0 : No t a Co mbinatio n Pro duct 0 3/0 1/20 20 0 2 NDC:74772-0 10 - 30 0 mL in 1 BOTTLE, SPRAY; Type 0 : No t a Co mbinatio n 3 0 3/0 1/20 20 0 3 Pro duct Marketing Information Marke ting Cate gory Application Numbe r or Monograph Citation Marke ting Start Date Marke ting End Date unappro ved drug o ther 0 3/0 1/20 20 Labeler - FORMULA (695075306) Registrant - FORMULA (695075306) Establishment Name Addre ss ID/FEI Busine ss Ope rations Daraewo rld Co ., Ltd. 6 8 9 9 0 0 0 25 manufacture(74772-0 10 ) Revised: 4/2020 FORMULA.
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