Label: REFREE HAND SANITIZER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 74002-5040-1, 74002-5040-2 - Packager: DONGBANGCOSMETICS CO.,LTD
- 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 April 18, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
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WARNINGS
Warnings:
For external use only. Flammable. Keep away from heat or flame
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Do not use
• in children less than 2 months of age
• on open skin wounds
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When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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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
- Uses
- Directions
- Other Information
- PACKAGE LABEL - REFREE HAND SANITIZER 30mL
- PACKAGE LABEL - REFREE HAND SANITIZER 500mL
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INGREDIENTS AND APPEARANCE
REFREE HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74002-5040 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 68 g in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) TROLAMINE (UNII: 9O3K93S3TK) lavender oil (UNII: ZBP1YXW0H8) hexylene glycol (UNII: KEH0A3F75J) STRAWBERRY SEED OIL (UNII: 9I73N69W76) GREEN TEA LEAF (UNII: W2ZU1RY8B0) Butylene Glycol (UNII: 3XUS85K0RA) GRAPEFRUIT OIL (UNII: YR377U58W9) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74002-5040-1 30 mL in 1 POUCH; Type 0: Not a Combination Product 04/01/2020 2 NDC:74002-5040-2 500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 04/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 04/01/2020 Labeler - DONGBANGCOSMETICS CO.,LTD (694452564) Registrant - DONGBANGCOSMETICS CO.,LTD (694452564) Establishment Name Address ID/FEI Business Operations DONGBANGCOSMETICS CO.,LTD 694452564 manufacture(74002-5040)