Label: SANITIZING ISOPROPYL ALCOHOL WIPES- hand sanitizer cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 78553-3920-1 - Packager: Unitrex Ltd.
- Category: HUMAN OTC DRUG LABEL
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 August 27, 2020
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
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WHEN USING
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. - STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
SANITIZING ISOPROPYL ALCOHOL WIPES
hand sanitizer clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:78553-3920 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 75 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 25 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:78553-3920-1 370 g in 1 CAN; Type 0: Not a Combination Product 08/27/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/27/2020 Labeler - Unitrex Ltd. (062032343) Registrant - Unitrex Ltd. (062032343) Establishment Name Address ID/FEI Business Operations Hangzhou Wellbeing Technology Co., Ltd. 414010999 manufacture(78553-3920)