Label: JOYDEN PLUS- chlorine dioxide liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 76769-0002-1 - Packager: Private company NEOCL
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated April 28, 2020
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
For external use only.
Flammable, keep away from fire or flame.
When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.
Stop use and ask a doctor if significant irritation or sensitization develops.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
JOYDEN PLUS
chlorine dioxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76769-0002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORINE DIOXIDE (UNII: 8061YMS4RM) (CHLORINE DIOXIDE - UNII:8061YMS4RM) CHLORINE DIOXIDE 0.3 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76769-0002-1 20000 mL in 1 CONTAINER; Type 0: Not a Combination Product 04/11/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/11/2020 Labeler - Private company NEOCL (695730456) Registrant - Private company NEOCL (695730456) Establishment Name Address ID/FEI Business Operations Private company NEOCL 695730456 manufacture(76769-0002)