Label: ZERO HAND SANITIZER- rosemary, chamomile, melaleuca alternifolia leaf, lavandula angustifolia liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 74772-010-01, 74772-010-02, 74772-010-03 - Packager: FORMULA
- 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 April 8, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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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
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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
- Uses
- Directions
- PACKAGE LABEL - ZERO Hand Sanitizer 60mL Spray
- PACKAGE LABEL - ZERO Hand Sanitizer 300mL Gel
- PACKAGE LABEL - ZERO Hand Sanitizer 300mL Spray
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INGREDIENTS AND APPEARANCE
ZERO HAND SANITIZER
rosemary, chamomile, melaleuca alternifolia leaf, lavandula angustifolia liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74772-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ROSEMARY (UNII: IJ67X351P9) (ROSEMARY - UNII:IJ67X351P9) ROSEMARY 1.0 g in 100 mL CHAMOMILE (UNII: FGL3685T2X) (CHAMOMILE - UNII:FGL3685T2X) CHAMOMILE 1.0 g in 100 mL MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K) (MELALEUCA ALTERNIFOLIA LEAF - UNII:G43C57162K) MELALEUCA ALTERNIFOLIA LEAF 1.0 g in 100 mL LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M) (LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER - UNII:19AH1RAF4M) LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER 1.0 g in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Butylene Glycol (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74772-010-01 60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/01/2020 2 NDC:74772-010-02 300 mL in 1 CONTAINER; Type 0: Not a Combination Product 03/01/2020 3 NDC:74772-010-03 300 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/01/2020 Labeler - FORMULA (695075306) Registrant - FORMULA (695075306) Establishment Name Address ID/FEI Business Operations Daraeworld Co., Ltd. 689900025 manufacture(74772-010)