Label: MEDIQUE COLDEEZE- zinc gluconate lozenge
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Contains inactivated NDC Code(s)
NDC Code(s): 47682-758-73 - Packager: Unifirst-First Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated March 10, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient (per lozenge)
- Purpose
- Uses
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Warnings
Do not use
for treatment of influenza or allergies. This product is intended only to reduce the duration of the common cols and its symptoms.
- If pregnant or breast-feeding,
- Keep out of reach of children.
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Directions
- take one lozenge at the onset of symptoms
- dissolve entire lozenge in mouth
- do not chew
- do not swallow whole
- do not eat or drink for 15 minutes after use
- repeat every 2 - 4 hours until symptoms subside
Adults 18 years and over: do not exceed 6 lozenges per day
Children 12 years to under 18 years: do not exceed 4 lozenges per day
Children under 12 years: ask a doctor before use
- Other information
- Inactive ingredients
- Questions or comments?
- Medique Principal Display Panel
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INGREDIENTS AND APPEARANCE
MEDIQUE COLDEEZE
zinc gluconate lozengeProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-758 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC GLUCONATE (UNII: U6WSN5SQ1Z) (ZINC CATION - UNII:13S1S8SF37) ZINC GLUCONATE 2 [hp_X] Inactive Ingredients Ingredient Name Strength CORN SYRUP (UNII: 9G5L16BK6N) GLYCINE (UNII: TE7660XO1C) SUCROSE (UNII: C151H8M554) Product Characteristics Color white ((Semi-Translucent)) Score no score Shape OVAL Size 23mm Flavor CHERRY Imprint Code P Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47682-758-73 25 in 1 BOX; Type 0: Not a Combination Product 03/17/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/17/2020 Labeler - Unifirst-First Aid Corporation (832947092) Establishment Name Address ID/FEI Business Operations Medique Products 086911794 relabel(47682-758) , repack(47682-758)