Label: CLEAN ON HAND SANITIZER PLUS- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 74522-030-01, 74522-030-02 - Packager: Caolion Cosmetics 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 June 10, 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 INGREDIENTS
- PURPOSE
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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: CLEAN ON HAND SANITIZER GEL PLUS 1gal
- Package Label: CLEAN ON HAND SANITIZER GEL PLUS 5L
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INGREDIENTS AND APPEARANCE
CLEAN ON HAND SANITIZER PLUS
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74522-030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) Alcohol 0.7 kg in 1 L Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) TROLAMINE (UNII: 9O3K93S3TK) Glycerin (UNII: PDC6A3C0OX) Propylene Glycol (UNII: 6DC9Q167V3) Panthenol (UNII: WV9CM0O67Z) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) ALOE VERA LEAF (UNII: ZY81Z83H0X) HYALURONATE SODIUM (UNII: YSE9PPT4TH) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74522-030-01 3.78 L in 1 BOTTLE; Type 0: Not a Combination Product 06/01/2020 2 NDC:74522-030-02 5 L in 1 BOTTLE; Type 0: Not a Combination Product 06/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 06/01/2020 Labeler - Caolion Cosmetics Co., Ltd. (557792513) Registrant - Caolion Cosmetics Co., Ltd. (557792513) Establishment Name Address ID/FEI Business Operations KOREA COSPACK CO.,LTD. 689059789 manufacture(74522-030)