Label: LFG- chloroxylenol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 77879-006-00 - Packager: BT Supplies West Inc
- 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 February 9, 2022
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- Drug Facts
- Active Ingredient
- Uses
- Warnings
- Directions
- Inactive Ingredients
- Package Labeling:
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INGREDIENTS AND APPEARANCE
LFG
chloroxylenol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77879-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 3 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) COCOYL METHYL MONOETHANOLAMINE (UNII: 79G1T427CF) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) GLYCERIN (UNII: PDC6A3C0OX) SODIUM CITRATE (UNII: 1Q73Q2JULR) SODIUM CHLORIDE (UNII: 451W47IQ8X) TOCOPHEROL (UNII: R0ZB2556P8) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ALCOHOL (UNII: 3K9958V90M) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) MAGNESIUM NITRATE (UNII: 77CBG3UN78) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77879-006-00 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/15/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 11/15/2020 Labeler - BT Supplies West Inc (033878488) Establishment Name Address ID/FEI Business Operations Zhejiang iColor Biotech Co., Ltd 554528308 manufacture(77879-006)