Label: THE ORIGINAL NATURAL HERB COUGH DROPS- menthol lozenge
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NDC Code(s):
63667-955-10,
63667-955-15,
63667-955-21,
63667-955-26, view more63667-955-27, 63667-955-45, 63667-955-50, 63667-955-65, 63667-955-90, 63667-955-93, 63667-955-95
- Packager: Ricola USA Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 22, 2025
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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
- Other Information
- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
THE ORIGINAL NATURAL HERB COUGH DROPS
menthol lozengeProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63667-955 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 SUCROSE (UNII: C151H8M554) CARAMEL (UNII: T9D99G2B1R) Product Characteristics Color brown (NUT BROWN) Score no score Shape RECTANGLE Size 16mm Flavor Imprint Code ; Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63667-955-21 21 in 1 BAG; Type 0: Not a Combination Product 01/01/1942 2 NDC:63667-955-65 65 in 1 BAG; Type 0: Not a Combination Product 01/01/1942 3 NDC:63667-955-95 105 in 1 BAG; Type 0: Not a Combination Product 01/01/1942 4 NDC:63667-955-90 90 in 1 BAG; Type 0: Not a Combination Product 06/01/2024 5 NDC:63667-955-10 10 in 1 BAG; Type 0: Not a Combination Product 01/01/1942 6 NDC:63667-955-15 115 in 1 BAG; Type 0: Not a Combination Product 01/01/1942 7 NDC:63667-955-26 26 in 1 BAG; Type 0: Not a Combination Product 01/01/1942 01/01/2016 8 NDC:63667-955-50 50 in 1 BAG; Type 0: Not a Combination Product 01/01/1942 9 NDC:63667-955-45 45 in 1 BAG; Type 0: Not a Combination Product 01/01/1942 10 NDC:63667-955-93 130 in 1 BAG; Type 0: Not a Combination Product 01/01/1942 11 NDC:63667-955-27 27 in 1 BAG; Type 0: Not a Combination Product 01/01/1942 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 01/01/1942 Labeler - Ricola USA Inc. (177265261) Establishment Name Address ID/FEI Business Operations Ricola Ag 485393768 manufacture(63667-955)