Label: DR. NATURE HUB- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 76901-010-01 - Packager: SHIMIZU 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 May 14, 2020
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENTS
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR. NATURE HUB
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76901-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) Alcohol 350 mL in 500 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) Glycerin (UNII: PDC6A3C0OX) TROLAMINE (UNII: 9O3K93S3TK) Allantoin (UNII: 344S277G0Z) Dexpanthenol (UNII: 1O6C93RI7Z) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) LAVENDER OIL (UNII: ZBP1YXW0H8) ASIAN GINSENG (UNII: CUQ3A77YXI) Orange Oil (UNII: AKN3KSD11B) LIMONENE, (+)- (UNII: GFD7C86Q1W) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76901-010-01 500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 05/01/2020 Labeler - SHIMIZU CO., LTD. (694646122) Registrant - SHIMIZU CO., LTD. (694646122) Establishment Name Address ID/FEI Business Operations Korea Miracle People Corporation Co.,Ltd 693710617 manufacture(76901-010)