SCOT-TUSSIN ORIGINAL SF MULTI-SYMPTOM- acetominophen, phenylephrine hydrochloride and pheniramine maleate liquid 
SCOT-TUSSIN Pharmacal Co., Inc.

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.

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Scot-Tussin Original SF Multi-Symptom

Active Ingredient

(in each 5 mL. tsp. teaspoon)
Acetaminophen USP 160 mg

Purpose

Pain reliever/Fever reducer

Active Ingredient

(in each 5 mL. tsp. teaspoon)
Pheniramine Maleate USP 4 mg

Purpose

Antihistamine

Active Ingredient

(in each 5 mL. tsp. teaspoon)
Phenylephrine HCI USP 4 mg

Purpose

Decongestant

Uses

Warnings

DO NOT USE THIS PRODUCT TO SEDATE CHILDREN

Liver warning: This product contains acetaminophne. Severe liver damange may occur if you take:

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.
  • if you are now taking a prescription monoamie 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 MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if you have

  • liver disease.
  • heart disease.
  • high blood pressure.
  • thyroid disease.
  • diabetes.
  • glaucoma.
  • a breathing problem such as emphysema, asthma or chronic broncititis.
  • trouble uritinating due to an enlarged prostate gland.

Ask a doctor or pharmacist before use if you are

  • taking sedatives or tranquilizers.
  • taking the blood thinning drug warfarin.

When using this product

  • do not use more than directed.
  • avoid alcoholic drinks.
  • drowsiness may occur.
  • alcohol, sedatives and tranquilizers may increase drowsiness.
  • be careful when driving a motor vehicle or operating machinery.
  • excitability may occur, especially in children.

Stop use and ask a doctor if

  • you get nervous, dizzy or sleepless.
  • pain or nasal congestion 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.
  • sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting.

If pregnant or breast-feeding,

Do Not Use

Keep out of reach of children.

In case of overdose get medical help or contact a Poison Control Center right away. Quick medical attention is critical for adults as well as children even if you do not notice any signs or symptoms.

Directions

agedose
Adults and children
over 12 years old
2 teaspoons
(2 tsp. 10ml.)
every 6 hours
Children under
12 years old
DO NOT USE

Other Information

Inactive Ingredients

ammonium glycyrrhizate, citric acid, clear cherry-strawberry flavor, glycerin, hydroxyethylcellulose, methyl paraben, polyethylene glycol, potassium benzoate, potassium citrate, propyl paraben, purified water, sucralose.

PRINCIPAL DISPLAY PANEL

SCOT-
TUSSIN
MULTI-SYMPTOM
COLD & ALLERGY

SCOT-
TUSSIN
MULTI-SYMPTOM
COLD & ALLERGY

SCOT-TUSSIN ORIGINAL SF MULTI-SYMPTOM 
acetominophen, phenylephrine hydrochloride and pheniramine maleate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0372-0004
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN160 mg  in 5 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE4 mg  in 5 mL
PHENIRAMINE MALEATE (UNII: NYW905655B) (PHENIRAMINE - UNII:134FM9ZZ6M) PHENIRAMINE MALEATE4 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
POTASSIUM BENZOATE (UNII: 763YQN2K7K)  
POTASSIUM CITRATE (UNII: EE90ONI6FF)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
Color    Score    
ShapeSize
FlavorCHERRY, STRAWBERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0372-0004-04118 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34112/01/1956
Labeler - SCOT-TUSSIN Pharmacal Co., Inc. (001203918)

Revised: 1/2013
Document Id: c863b9be-68be-404d-8a21-16237bbcf43e
Set id: f142eec2-1764-4086-b24e-fbff358ed8df
Version: 6
Effective Time: 20130125
 
SCOT-TUSSIN Pharmacal Co., Inc.