Label: EPU HAND SANITIZER 946ML- ethyle alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 73862-217-10, 73862-217-11 - Packager: E.CIS Cosmetic Co.,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 June 17, 2020
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
EPU HAND SANITIZER 946ML
ethyle alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73862-217 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength AMINOMETHYLPROPANOL (UNII: LU49E6626Q) MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N) PANTHENOL (UNII: WV9CM0O67Z) GLYCERIN (UNII: PDC6A3C0OX) CARBOMER 940 (UNII: 4Q93RCW27E) WATER (UNII: 059QF0KO0R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALOE VERA LEAF (UNII: ZY81Z83H0X) HYALURONATE SODIUM (UNII: YSE9PPT4TH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73862-217-11 12 in 1 CASE 03/30/2020 1 NDC:73862-217-10 946 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/30/2020 Labeler - E.CIS Cosmetic Co.,Ltd (689846270) Registrant - E.CIS Cosmetic Co.,Ltd (689846270) Establishment Name Address ID/FEI Business Operations E.CIS Cosmetic Co.,Ltd 689846270 manufacture(73862-217)