SANATOS MULTI SYMPTOM DAYTIME- acetaminophen, dextromethorphan hbr liquid 
Pharmadel LLC

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Sanatos Daytime MS 6 (PLE)

Drug Facts

Active ingredients & Purposes

Active ingredients

(in each 30 mL)

Purposes
Acetaminophen 650 mg Pain reliever/ fever reducer
Dextromethorphan HBr 20 mgCough suppressant

Uses

Temporarily relieves common cold/flu symptoms associted with

Warnings

Liver warning: This product contains acetaminophen. Severe liver damage may occur if

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

  • 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.
  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.

Ask a doctor before use if user

  • has a sodium restricted diet
  • has liver disease
  • hastrouble urinating due to enlarged prostate gland
  • haspersistent or chronic cough such as occurs with smoking, asthma, or emphysema
  • has a cough that occurs with too much phlegm (mucus)
  • is a child with pain of arthritis


Ask a doctor or pharmacist before use if the user is

  • taking the blood thinning drug warfarin

Stop use and ask a doctor if

  • pain or cough gets worse or lasts more than 5 days (children) or 7 days (adults)
  • fever gets worse or lasts more than 3 days
  • redness or swelling is present
  • new symptoms occur
  • cough comes back or occurs with 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. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

adults & children 12 years & over30 mL every 4 hours, do not exceed (child) 4 doses and (adult) 6 doses per 24 hours
children under 12 years of agedo not use

Other information

TAMPER EVIDENT: Do not use if imprinted band is missing or broken.

Inactive ingredients

citric acid anhydrous, FD&C yellow #6, flavor, glycerin, menthol, propylene glycol, sodium benzoate, sorbitol solution, sodium citrate, sucralose, xanthan gum, water

Questions?

+1-866-359-3478 (M-F) 9AM – 5PM EST or www.pharmadel.com

Distributed by:

Pharmadel LLC

New Castle, DE 19720

www.pharmadel.com

Facebook/PHARMADELUSA

Prinicipal Display Panel

PDP Sanatos MS Day

SANATOS  MULTI SYMPTOM DAYTIME
acetaminophen, dextromethorphan hbr liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55758-415
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg  in 30 mL
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN650 mg  in 30 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
WATER (UNII: 059QF0KO0R)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
SORBITOL SOLUTION (UNII: 8KW3E207O2)  
XANTHAN GUM (UNII: TTV12P4NEE)  
MENTHOL (UNII: L7T10EIP3A)  
Product Characteristics
Colororange (Yellow Orange) Score    
ShapeSize
FlavorCHERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55758-415-06177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01312/01/2023
Labeler - Pharmadel LLC (030129680)

Revised: 12/2023
Document Id: 0a5fc0ef-ba33-bb0b-e063-6394a90af7d9
Set id: 0a5fc0ef-ba34-bb0b-e063-6394a90af7d9
Version: 1
Effective Time: 20231201
 
Pharmadel LLC