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. Updated January 12, 2022 If you are a consumer or patient please visit this version.Drug Label Information
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
- heart disease
- diabetes
- high blood pressure
- thyroid disease
- trouble urinating due to an enlarged prostate gland
- persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema
- cough that occurs with too much phlegm (mucus)
When using this product do not use more than directed
Stop use and ask a doctor if
- nervousness, dizziness, or sleeplessness occur
- symptoms do not get better within 7 days or occur with fever
- cough comes back, or occurs with fever, rash, or headache that lasts. These could be signs of a serious condition.
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center right away.
- do not take more than 12 caplets in any 24-hour period
- adults and children 12 years of age and over: take 2 caplets every 4 hours
- children under 12 years of age: do not use
- store at 20-25°C (68-77°F)
croscarmellose sodium, FD&C blue no. 2 aluminum lake, FD&C red no. 40 aluminum lake, methacrylic acid-ethyl acrylate copolymer, mica, microcrystalline cellulose, polyethylene glycol 3350, polysorbate 80, polyvinyl alcohol, povidone K29/32, sodium bicarbonate, talc, titanium dioxide
1-866-MUCINEX (1-866-682-4639) You may also report side effects to this phone number.
Dist. by: RB Health (US)
Parsippany, NJ 07054-0224
MAXIMUM STRENGTH
NDC 63824-193-21
Mucinex®
FAST-MAX®
SEVERE CONGESTION
& COUGH
Dextromethorphan HBr – Cough
Suppressant
Guaifenesin – Expectorant
Phenylephrine HCl – Nasal Decongestant
✓ Controls Cough
✓ Relieves Nasal & Chest Congestion
✓ Thins & Loosens Mucus
Actual Size
20 CAPLETS
FOR AGES 12+
View Labeling Archives for this drug
MUCINEX FAST-MAX SEVERE CONGESTION AND COUGH- dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride tablet, coated
Number of versions: 8
Jan 13, 2022 | 9 (current) | download |
Sep 16, 2020 | 8 | download |
Dec 11, 2018 | 7 | download |
Jan 4, 2016 | 6 | download |
Nov 5, 2015 | 5 | download |
Dec 5, 2014 | 3 | download |
Oct 28, 2014 | 2 | download |
Mar 15, 2013 | 1 | download |
RxNorm
MUCINEX FAST-MAX SEVERE CONGESTION AND COUGH- dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride tablet, coated
1 | 1372652 | dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet | PSN |
2 | 1372652 | dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet | SCD |
3 | 1372652 | dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine HCl 5 MG Oral Tablet | SY |
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NDC Codes
MUCINEX FAST-MAX SEVERE CONGESTION AND COUGH- dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride tablet, coated
If this SPL contains inactivated NDCs listed by the FDA initiated compliance action, they will be specified as such.
1 | 63824-193-20 |
2 | 63824-193-21 |
3 | 63824-193-30 |