Label: MOORE MEDICAL MENTHOL EUCALYPTUS COUGH DROPS- menthol cough drops lozenge
- NDC Code(s): 55670-060-25
- Packager: Moore Medical LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 April 20, 2022
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
- Purpose
- Uses
- Warnings
- Ask a doctor if you have
- Stop use and ask a doctor if
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- QUESTIONS
- Moore Medical Menthol Eucalyptus Cough Drops PDP Label
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INGREDIENTS AND APPEARANCE
MOORE MEDICAL MENTHOL EUCALYPTUS COUGH DROPS
menthol cough drops lozengeProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55670-060 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL 7 mg Inactive Ingredients Ingredient Name Strength CORN SYRUP (UNII: 9G5L16BK6N) EUCALYPTUS OIL (UNII: 2R04ONI662) SUCROSE (UNII: C151H8M554) Product Characteristics Color white (Translucent) Score no score Shape OVAL Size 23mm Flavor MENTHOL (Eucalyptus) Imprint Code P Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55670-060-25 125 in 1 JAR; Type 7: Separate Products Requiring Cross Labeling 02/01/2016 08/30/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 02/01/2016 08/30/2024 Labeler - Moore Medical LLC (051420107) Registrant - Unifirst First Aid Corporation (832947092)