Label: GAO BEN F ADVANCED HAND SANITIZER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 76683-010-01, 76683-010-02 - Packager: KRIBS 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 27, 2020
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
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WARNINGS
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
- Uses
- Directions
- Other information
- Questions
- PACKAGE LABEL : GAO-BEN F ADVANCED HAND SANITIZER GEL 50mL
- PACKAGE LABEL : GAO-BEN F ADVANCED HAND SANITIZER GEL 500mL
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INGREDIENTS AND APPEARANCE
GAO BEN F ADVANCED HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76683-010 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 Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) TROLAMINE (UNII: 9O3K93S3TK) TURMERIC (UNII: 856YO1Z64F) ALOE VERA LEAF (UNII: ZY81Z83H0X) ORANGE OIL (UNII: AKN3KSD11B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76683-010-01 50 mL in 1 CONTAINER; Type 0: Not a Combination Product 04/01/2020 2 NDC:76683-010-02 500 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 - KRIBS Co., Ltd. (695625841) Registrant - KRIBS Co., Ltd. (695625841) Establishment Name Address ID/FEI Business Operations KRIBS Co., Ltd. 695625841 manufacture(76683-010)