Label: SUGAR FREE ORIGINAL SWISS HERB COUGH SUPPRESSANT THROAT DROPS- menthol lozenge
- NDC Code(s): 54305-802-19, 54305-802-24, 54305-802-45
- Packager: Ricola Ag
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 5, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient (in each drop)
- Uses
- Warnings
- Ask doctor before use if you have
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
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Other Information
- Phenylketonurics: contains phenylalanine 1 mg per drop
- excessive use may have a laxative effect
- store in a dry place
- product may be useful for diabetics on the advice of a doctor
Exchange information: 2 Drops = FREE Exchange
7 Drops = 1 Fruit
Dietary exchanges based on Exchange Lists for Diabetics
© 2008 American Diabetes Association, American Dietetic Association
- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SUGAR FREE ORIGINAL SWISS HERB COUGH SUPPRESSANT THROAT DROPS
menthol lozengeProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54305-802 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 4.8 mg Inactive Ingredients Ingredient Name Strength ISOMALT (UNII: S870P55O2W) SORBITOL (UNII: 506T60A25R) ASPARTAME (UNII: Z0H242BBR1) CARAMEL (UNII: T9D99G2B1R) Product Characteristics Color brown (DEER BROWN) Score no score Shape OVAL Size 24mm Flavor MENTHOL Imprint Code R Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54305-802-19 19 in 1 BAG; Type 0: Not a Combination Product 04/12/1942 2 NDC:54305-802-24 24 in 1 BAG; Type 0: Not a Combination Product 04/12/1942 12/29/2017 3 NDC:54305-802-45 45 in 1 BAG; Type 0: Not a Combination Product 04/12/1942 12/29/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 04/12/1942 Labeler - Ricola Ag (480227248) Establishment Name Address ID/FEI Business Operations Ricola Ag 485393768 manufacture(54305-802)