Label: BISOLVINE ALOE-MIEL- dextromethorphan, guaifenesin liquid
- NDC Code(s): 53145-402-06
- Packager: MENPER DISTRIBUTORS INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 22, 2025
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- Official Label (Printer Friendly)
- Active Ingredients (in each 15 mL)
- Purpose
- Uses
- Do not exceed recommended dosage.
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Do not use:
* this product for persistent or chronic cough, such as occurs with smoking, asthma, chronic bronchitis, or emphysema or where cough is accompanied by excessive phlegm (mucus), unless directed by a doctor.
* If you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's Disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. - KEEP OUT OF REACH OF CHILDREN
- PREGNANCY OR BREAST FEEDING
- Directions
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Inactive Ingredients
Aloe leaf extract, ascorbic acid, caramel color, cat's claw bark extract, corn syrup, DATEM, ethyl alcohol, eucalyptus oil, flavor, garlic bulb extract, ginger root extract, gum arabic, honey, menthol, methylparaben, onion bulb extract, peppermint leaf extract, polysorbate 80, potassium sorbate, propylene glycol, propylparaben, sodium benzoate, sucralose, sunflower oil, and water.
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INGREDIENTS AND APPEARANCE
BISOLVINE ALOE-MIEL
dextromethorphan, guaifenesin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53145-402 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 10 mg in 15 mL GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 100 mg in 15 mL Inactive Ingredients Ingredient Name Strength ALOE (UNII: V5VD430YW9) ASCORBIC ACID (UNII: PQ6CK8PD0R) CAT'S CLAW (UNII: 9060PRM18Q) CORN SYRUP (UNII: 9G5L16BK6N) ALCOHOL (UNII: 3K9958V90M) EUCALYPTUS OIL (UNII: 2R04ONI662) GARLIC (UNII: V1V998DC17) GINGER (UNII: C5529G5JPQ) ACACIA (UNII: 5C5403N26O) HONEY (UNII: Y9H1V576FH) MENTHOL (UNII: L7T10EIP3A) METHYLPARABEN (UNII: A2I8C7HI9T) ONION (UNII: 492225Q21H) PEPPERMINT (UNII: V95R5KMY2B) POLYSORBATE 80 (UNII: 6OZP39ZG8H) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) SODIUM BENZOATE (UNII: OJ245FE5EU) SUCRALOSE (UNII: 96K6UQ3ZD4) SUNFLOWER OIL (UNII: 3W1JG795YI) WATER (UNII: 059QF0KO0R) DIACETYLTARTARIC AND FATTY ACID ESTERS OF GLYCEROL (UNII: 248HN3Z28U) CARAMEL (UNII: T9D99G2B1R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53145-402-06 1 in 1 CARTON 01/01/2019 1 180 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 01/01/2019 Labeler - MENPER DISTRIBUTORS INC. (101947166) Establishment Name Address ID/FEI Business Operations RNV, LLC 118917568 manufacture(53145-402)

