Label: JOYDEN- chlorine dioxide liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 76769-0003-1, 76769-0003-2, 76769-0003-3 - Packager: Private company NEOCL
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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 October 27, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- 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
Keep out of reach of children
Do not use
In children less than 2 months of age
On open skin wounds
For other than intended purpose
Avoid contact with eye. If contact occurs, rinse cautiously with water for several minutes.
Remove contact lenses. Continue rising.
If eye irritation persists, get medical advice/attention.
Store at room temperature and avoid direct sunlight
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
JOYDEN
chlorine dioxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76769-0003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORINE DIOXIDE (UNII: 8061YMS4RM) (CHLORINE DIOXIDE - UNII:8061YMS4RM) CHLORINE DIOXIDE 0.003 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:76769-0003-1 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/27/2020 2 NDC:76769-0003-2 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/27/2020 3 NDC:76769-0003-3 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/27/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/27/2020 Labeler - Private company NEOCL (695730456) Registrant - Private company NEOCL (695730456) Establishment Name Address ID/FEI Business Operations Private company NEOCL 695730456 manufacture(76769-0003)
