Label: RELIABLE GOLD ANTIMICROBIAL LTION SO AP- chloroxylenol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 71897-051-27, 71897-051-37 - Packager: Veritiv Operating Company
- 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 August 30, 2017
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- Active ingredient
- Purpose
- Use
- Warnings
- Directions
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RELIABLE GOLD ANTIMICROBIAL LTION SO AP
chloroxylenol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71897-051 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Chloroxylenol (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) Chloroxylenol 0.003 mg in 1 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Coconut Acid (UNII: 40U37V505D) Oleic Acid (UNII: 2UMI9U37CP) Sodium Sulfate (UNII: 0YPR65R21J) MONOETHANOLAMINE (UNII: 5KV86114PT) COCO MONOETHANOLAMIDE (UNII: C80684146D) Coco-Betaine (UNII: 03DH2IZ3FY) Propylene Glycol (UNII: 6DC9Q167V3) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) EDETATE SODIUM (UNII: MP1J8420LU) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CORN OIL (UNII: 8470G57WFM) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71897-051-27 800 mL in 1 PACKAGE; Type 0: Not a Combination Product 01/31/2003 2 NDC:71897-051-37 3780 mL in 1 PACKAGE; Type 0: Not a Combination Product 01/31/2003 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 01/31/2003 Labeler - Veritiv Operating Company (006989982)