NDC | 53942-504-26 |
Set ID | c19b9997-4037-48f3-b905-86da421a292d |
Category | HUMAN OTC DRUG LABEL |
Packager | DeMoulas Market Basket |
Generic Name | |
Product Class | alpha-1 Adrenergic Agonist |
Product Number | |
Application Number | PART341 |
- DRUG FACTSActive ingredients(in each 5 mL tsp)
- Purposes
- Keep out of reach of children
- Uses
-
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
Ask a doctor or pharmacist before use
- heart disease
- high blood pressure
- thyroid disease
- diabetes
- trouble urinating due to an enlarged prostate gland
- cough that occurs with too much phlegm mucus)
- cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema
Ask a doctor or pharmacist before use if you are taking any other oral nasal decongestant or stimulant.
When using this product do not use more than directed. - Stop use and ask a doctor if
- If pregnant or breast-feeding
- Directions
- Other information
- Inactive ingredients
- Questions?
-
Product Label
"MORE FOR YOUR DOLLAR"
MARKET BASKET®
*COMPARE TO THE ACTIVE INGREDIENTS IN ROBITUSSIN® PEAK COLD MULTI-SYMPTOM COLD
Tussin CF Multi-Symptom Cold
Dextromethorphan HBr/ Guaifenesin / Phenylephrine HCL
COUGH SUPPRESSANT
EXPECTORANT/
NASAL DECONGESTANTDO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING
Relieves:
- Cough
- Mucus
- Nasal Congestion
NON-DROWSY
ADULT
for ages 12 and over
8 FL OZ (237 mL)*This product is not manufactured or distributed by Pfizer, owner of the trademark Robitussin ®
DISTRIBUTED BY DEMOULAS SUPERMARKETS INC. 875 EAST STREET TEWKSBURG, MA 01876 BX-013
-
INGREDIENTS AND APPEARANCE
TUSSIN CF MULTI-SYMPTOM COLD
dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53942-504 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 5 mL GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 100 mg in 5 mL PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 5 mg in 5 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) FD&C RED NO. 40 (UNII: WZB9127XOA) GLYCERIN (UNII: PDC6A3C0OX) MENTHOL (UNII: L7T10EIP3A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) SORBITOL (UNII: 506T60A25R) SUCRALOSE (UNII: 96K6UQ3ZD4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53942-504-26 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/20/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 09/20/2012 Labeler - DeMoulas Market Basket (007869647) Registrant - DeMoulas Market Basket (007869647) Establishment Name Address ID/FEI Business Operations AptaPharma Inc. 790523323 manufacture(53942-504)