Label: BONANGE HAND CLEANER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 75005-030-01, 75005-030-02 - Packager: Mi-face 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 9, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
INACTIVE INGREDIENTS:
Water, Glycerin, Phenoxyethanol, Carbomer, Triethanolamine, Butylene Glycol, 1,2-Hexanediol, PEG-60 Hydrogenated Castor Oil, Lavandula Angustifolia (Lavender) Oil, Opuntia Ficus-Indica Extract, Bambusa Vulgaris Leaf/Stem Extract, Avena Sativa (Oat) Kernel Extract, Luffa Cylindrica Fruit Extract, Aloe Barbadensis Leaf Extract, Salvia Hispanica Seed Extract, Cocos Nucifera (Coconut) Fruit Extract, Butyrospermum Parkii (Shea) Butter Extract, Scutellaria Baicalensis Extract, Laminaria Japonica Extract, Ethylhexylglycerin
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- Uses:
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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. - Directions
- Other Information
- Package Label: BONANGE HAND CLEANER 3mL * 100ea
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INGREDIENTS AND APPEARANCE
BONANGE HAND CLEANER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75005-030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 1.86 mL in 3 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Phenoxyethanol (UNII: HIE492ZZ3T) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) Trolamine (UNII: 9O3K93S3TK) Butylene Glycol (UNII: 3XUS85K0RA) 1,2-Hexanediol (UNII: TR046Y3K1G) PEG-60 Hydrogenated Castor Oil (UNII: 02NG325BQG) LAVENDER OIL (UNII: ZBP1YXW0H8) OPUNTIA FICUS-INDICA WHOLE (UNII: 23Z87HTQ6P) BAMBUSA VULGARIS TOP (UNII: FIW80T6P6V) OAT (UNII: Z6J799EAJK) LUFFA AEGYPTIACA FRUIT (UNII: QKL9NEO1F9) ALOE VERA LEAF (UNII: ZY81Z83H0X) CHIA SEED (UNII: NU0OLX06F8) COCONUT (UNII: 3RT3536DHY) SHEA BUTTER (UNII: K49155WL9Y) SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) LAMINARIA JAPONICA (UNII: WE98HW412B) Ethylhexylglycerin (UNII: 147D247K3P) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75005-030-02 100 in 1 CARTON 05/01/2020 1 NDC:75005-030-01 3 mL in 1 POUCH; 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 part333E 05/01/2020 Labeler - Mi-face Co., Ltd (694820628) Registrant - Mi-face Co., Ltd (694820628) Establishment Name Address ID/FEI Business Operations Mi-face Co., Ltd 694820628 manufacture(75005-030)
