Label: MUCUS RELIEF DM- dextromethorphan hydrobromide guaifenesin liquid
- NDC Code(s): 30142-508-06
- Packager: The Kroger Co.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated June 10, 2024
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- Official Label (Printer Friendly)
- Active ingredients (in each 20 mL)
- Purpose
- Uses
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Warnings
Do not use
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.
Ask a doctor before use if you have
- persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema
- cough accompanied by too much phlegm (mucus)
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Directions
- do not take more than 6 doses in any 24-hour period
- measure only with dosing cup provided. Do not use any other device
- keep dosing cup with product
- mL = milliliter
- dose as follows or as directed by a doctor
- adults and children 12 years of age and older: 20 mL every 4 hours
- children under 12 years of age: do not use
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
COMPARE TO the active ingredients of MUCINEX® FAST-MAX® DM MAX
for ages 12+
maximum Strength
FAST
Mucus Relief
DM Max
multi-Symptom
Dextromethorphan HBr 20 mg
Cough Suppressant
Guaifenesin 400 mg
Expectorant
Relieves
Chest Congestion
Controls Cough
Thin & Loosens Mucus
4 Hour Dosing
*Mucinex® Fast-Max® DM Max is a registered trademark of Reckitt Benckiser, Slough, UK. Reckitt Benckiser is not affiliated with The Kroger Co. or this product
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.
DISTRIBUTED BY: THE KROGER CO.
CINCINNATI, OHIO 45202
- Package Label
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INGREDIENTS AND APPEARANCE
MUCUS RELIEF DM
dextromethorphan hydrobromide guaifenesin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-508 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 20 mg in 20 mL GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 400 mg in 20 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) EDETATE DISODIUM (UNII: 7FLD91C86K) FD&C RED NO. 40 (UNII: WZB9127XOA) GLYCERIN (UNII: PDC6A3C0OX) PROPYL GALLATE (UNII: 8D4SNN7V92) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K) SORBITOL (UNII: 506T60A25R) SUCRALOSE (UNII: 96K6UQ3ZD4) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30142-508-06 177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 09/01/2020 Labeler - The Kroger Co. (006999528)