Label: SUCRETS VAPOR CHERRY- dyclonine hydrochloride and menthol lozenge
- NDC Code(s): 63736-921-18
- Packager: Insight Pharmaceuticals LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 June 22, 2018
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (per lozenge)
- Purpose
- Uses
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Warnings
Sore throat warning: if sore throat is severe, persists for more than 2 days, is accompanied by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly.
- Directions
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SUCRETS VAPOR CHERRY
dyclonine hydrochloride and menthol lozengeProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63736-921 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DYCLONINE HYDROCHLORIDE (UNII: ZEC193879Q) (DYCLONINE - UNII:078A24Q30O) DYCLONINE HYDROCHLORIDE 2 mg MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 6 mg Inactive Ingredients Ingredient Name Strength ASCORBIC ACID (UNII: PQ6CK8PD0R) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CORN SYRUP (UNII: 9G5L16BK6N) FD&C RED NO. 40 (UNII: WZB9127XOA) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM ASCORBATE (UNII: S033EH8359) TARTARIC ACID (UNII: W4888I119H) WATER (UNII: 059QF0KO0R) ZINC GLUCONATE (UNII: U6WSN5SQ1Z) Product Characteristics Color RED Score no score Shape OVAL Size 19mm Flavor CHERRY Imprint Code S;Vapor;Cherry Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63736-921-18 18 in 1 CANISTER; Type 0: Not a Combination Product 07/28/2009 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part356 07/28/2009 Labeler - Insight Pharmaceuticals LLC (055665422)