NDC | 58602-110-18, 58602-110-21 |
Set ID | ad8c993d-374c-4fb4-9e57-a4bdc0b7fe47 |
Category | Human OTC Drug Label |
Packager | Aurohealth LLC |
Generic Name | |
Product Class | alpha-1 Adrenergic Agonist |
Product Number | |
Application Number | PART341 |
- Drug Facts
- Purposes
-
Uses
- temporarily relieves these common cold and flu symptoms:
- cough
- nasal congestion
- sinus congestion and pressure
- minor aches and pains
- sore throat
- headache
- temporarily reduces fever
- temporarily promotes nasal and/or sinus drainage
- helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive
- temporarily relieves these common cold and flu symptoms:
-
Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:
- more than 4,000 mg of acetaminophen in 24 hours
- with other drugs containing acetaminophen
- 3 or more alcoholic drinks daily while using this product
Allergy alert: acetaminophen may cause severe skin reactions. Symptoms may include:
- skin reddening
- blisters
- rash
If a skin reaction occurs, stop use and seek medical help right away.
Sore throat warning: if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea or vomiting, consult a doctor promptly.
-
Do not use
- with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
- for children under 12 years of age
- 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.
- if you have ever had an allergic reaction to this product or any of its ingredients Avoid foods or beverages that contain caffeine
- Ask a doctor before use if you have
- Ask a doctor or pharmacist before use if
- When using this product
-
Stop use and ask a doctor if
- nervousness, dizziness or sleeplessness occur
- pain, nasal congestion or cough gets worse, or lasts more than 7 days
- fever gets worse, or lasts more than 3 days
- redness or swelling is present
- new symptoms occur
- 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,
-
Keep out of reach of children.
Overdose warning:
Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms. -
Directions
- do not take more than directed (see Overdose warning)
- measure only with dosing cup provided
- do not use dosing cup with other products
- dose as follows or as directed by a doctor
- mL = milliliter; tsp = teaspoon
- adults and children 12 years of age and older: 20 mL (4 tsp) orally every 4 hours, not to exceed 6 doses in 24 hours
- children under 12 years of age: do not use unless directed by a doctor
- Other information
- Inactive ingredients
- Questions or Comments
-
PACKAGE LABEL-PRINCIPAL DISPLAY PANEL 6 FL OZ (180 mL Bottle)
AUROHEALTH
NDC 58602-110-18
Compare to the active ingredients in
Mucinex® FAST-MAXTM
Cold, Flu & Sore Throat*
MAXIMUM STRENGTH**AuroMucus
Fast Maximum
Cold, Flu & Sore Throat Relief
Each dose 20 mL (4 tsp) of oral solution contains:
650 mg - Acetaminophen USP (Pain Reliever/Fever Reducer)
20 mg - Dextromethorphan HBr USP (Cough Suppressant)
400 mg - Guaifenesin USP (Expectorant)
10 mg - Phenylephrine HCl USP (Nasal Decongestant)
- Relieves Headache & Fever
- Controls Cough
- Relieves Nasal & Chest Congestion
- Thins & Loosens Mucus
For Ages 12+ 6 FL OZ (180 mL)
-
PACKAGE LABEL-PRINCIPAL DISPLAY PANEL 9 FL OZ (266 mL Bottle)
AUROHEALTH
NDC 58602-110-21
Compare to the active ingredients in
Mucinex® FAST-MAXTM
Cold, Flu & Sore Throat*
MAXIMUM STRENGTH**
AuroMucus
Fast Maximum
Cold, Flu & Sore Throat Relief
Each dose 20 mL (4 tsp) of oral solution contains:
650 mg - Acetaminophen USP (Pain Reliever/Fever Reducer)
20 mg - Dextromethorphan HBr USP (Cough Suppressant)
400 mg - Guaifenesin USP (Expectorant)
10 mg - Phenylephrine HCl USP (Nasal Decongestant)
- Relieves Headache & Fever
- Controls Cough
- Relieves Nasal & Chest Congestion
- Thins & Loosens Mucus
For Ages 12+ 9 FL OZ (266 mL)
-
INGREDIENTS AND APPEARANCE
AUROMUCUS - FAST MAXIMUM COLD, FLU AND SORE THROAT RELIEF
acetaminophen, dextromethorphan hydrobromide, guaifenesin and phenylephrine hydrochloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58602-110 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 650 mg in 20 mL 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 PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 10 mg in 20 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) EDETATE DISODIUM (UNII: 7FLD91C86K) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 40 (UNII: WZB9127XOA) PINEAPPLE (UNII: 2A88ZO081O) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYL GALLATE (UNII: 8D4SNN7V92) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) SORBITOL (UNII: 506T60A25R) SUCRALOSE (UNII: 96K6UQ3ZD4) XANTHAN GUM (UNII: TTV12P4NEE) Product Characteristics Color BLUE (Blue to Bluish Green) Score Shape Size Flavor BERRY, PINEAPPLE Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58602-110-18 180 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/03/2015 06/22/2022 2 NDC:58602-110-21 266 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/03/2015 06/22/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part341 07/03/2015 06/22/2022 Labeler - Aurohealth LLC (078728447) Establishment Name Address ID/FEI Business Operations Aurohealth LLC 078728447 MANUFACTURE(58602-110)