Label: QUASH MULTI SANITIZING TISSUE- alcohol cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 72265-104-01 - Packager: CURESCRIPT
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 February 9, 2021
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENTS
Water,Glycerin,Sodium Benzoate,PEG-60 Hydrogenated Castor Oil ,Fragrance,Citric acid,Menthol,1,2-Hexanediol,Poloxamer 184,PEG-7 Glyceryl Cocoate,Aloe Barbadensis Leaf Extract,Thymus Vulgaris (Thyme) Extract,Sophora Flavescens Root Extract,Sodium Hyaluronate,Cocamidopropyl Betaine,Butylene Glycol,Sodium Chloride
- PURPOSE
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WARNINGS
For external use only-hands
Flammable. Keep away from heat and flame.
When using this product ■ Keep out of eyes. In case of contact with eyes, flush thoroughly with water. ■ Avoid contact with broken skin. ■ Do not inhale or ingest.
Stop use and ask a doctor if skin irritation or rash develops.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- Other Information
- QUESTIONS
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
QUASH MULTI SANITIZING TISSUE
alcohol clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72265-104 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.54 Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Sodium Benzoate (UNII: OJ245FE5EU) PEG-60 Hydrogenated Castor Oil (UNII: 02NG325BQG) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Menthol (UNII: L7T10EIP3A) 1,2-Hexanediol (UNII: TR046Y3K1G) POLOXAMER 184 (UNII: BIS92ZSF57) PEG-7 Glyceryl Cocoate (UNII: VNX7251543) ALOE VERA LEAF (UNII: ZY81Z83H0X) THYME (UNII: CW657OBU4N) SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K) HYALURONATE SODIUM (UNII: YSE9PPT4TH) Cocamidopropyl Betaine (UNII: 5OCF3O11KX) Butylene Glycol (UNII: 3XUS85K0RA) Sodium Chloride (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72265-104-01 20 in 1 PACKET; Type 0: Not a Combination Product 02/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 02/01/2021 Labeler - CURESCRIPT (694894509) Registrant - CURESCRIPT (694894509) Establishment Name Address ID/FEI Business Operations Biostech Co., Ltd. 687294330 manufacture(72265-104)