SAFETUSSIN PM NIGHTTIME COUGH RELIEF- dextromethorphan hbr, doxylamine succinate liquid 
Kramer Laboratories

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Safetussin PM NightTime Cough Relief Drug Facts

Active ingredients (in each 5mL)

Purpose

Dextromethorphan HBr, USP 7.5 mg

Cough Suppressant

Doxylamine Succinate 3.125 mg

Antihistamine

Uses

temporarily relieves cough
runny nose and sneezing

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
.to make a child sleep.

Ask a doctor before use if you have

asthma
emphysema
glaucoma
excessive phlegm (mucus)
breathing problem
chronic bronchitis
persistent or chronic cough
cough associated with smoking
trouble urinating due to enlarged prostate gland
a sodium-restricted diet

Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers.

When using this product

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

Stop use and ask a doctor if cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. 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.

Directions

do not take more than 4 doses in any 24-hour period

age

dose

adults and children 12 years and over

20 mL every 6 hours

children under 12 years

ask a doctor

children under 4 years

do not use

Other information:

Protect from excessive heat and freezing. Store at 15° - 30° C (59° - 86° F) Save this package for complete information

Inactive ingredients:

citric acid, glycerin, menthol, natural peppermint flavor, propylene glycol, purified water, sodium benzoate, sucralose

PRINCIPAL DISPLAY PANEL

SAFE FOR ADULTS WITH

HIGH BLOOD PRESSURE & DIABETES

Safetussin® PM 
NightTime
Cough Relief
Dextromethorphan HBr 7.5 mg / Cough Suppressant

Doxylamine Succinate 3.125 mg / Antihistamine

Safe for adults with
High Blood Pressure
Diabetes

√ Controls Cough
√ Relieves Sneezing
√ Relieves runny nose

SUGAR & ALCOHOL FREE

4.0 FL OZ (118mL)


SEGURO PARA ADULTOS CON PRESION ALTA Y DIABETES

Safetussin® PM
Alivia la Tos
Durante la Noche

Dextromethorphan HBr 7.5 mg / Antiusivo

Doxylamine Succinate 3.125 mg / Antihistaminíco

Seguro para adultos con
Presión Alta
Diabetes

√ Calma la tos,
√ Alivia estornudos
√ Alivia goteo de la nariz
 
SIN AZÚCAR Y SIN ALCOHOL

4 FL. OZ (118 mL)

Safetussin® PM
NIGHT TIME
COUGH RELIEF
Cough Suppressant / Antihistamine

Up To
8 Hours of cough relief 
to help you rest

Safetussin® PM contains:

√ No decongestants

√ No acetaminophen

√ No sugar

√ No alcohol

√ No sorbitol

√ No fructose

√ No gluten

√ No dyes

Pharmacist Recommended Brand

Always read and follow label directions. Do not use longer than 7 consecutive days unless directed by a doctor. Ask a doctor if you have individual health questions.
Questions? Comments?
Call 1-800-824-4894 

© 2023 Kramer Laboratories, Inc.
Bridgewater, NJ 08807 ● kramerlabs.com
K0723

Safetussin PM NightTime Cough Relief 4.0 FL OZ (118 mL)
SAFETUSSIN PM NIGHTTIME  COUGH RELIEF
dextromethorphan hbr, doxylamine succinate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55505-221
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Dextromethorphan (UNII: 7355X3ROTS) (Dextromethorphan - UNII:7355X3ROTS) Dextromethorphan Hydrobromide7.5 mg  in 5 mL
DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2) (DOXYLAMINE - UNII:95QB77JKPL) DOXYLAMINE SUCCINATE3.125 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
GLYCERIN (UNII: PDC6A3C0OX)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
MINT (UNII: FV98Z8GITP)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
water (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
Product Characteristics
Color    Score    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55505-221-331 in 1 CARTON07/28/2023
1118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01207/28/2023
Labeler - Kramer Laboratories (122720675)

Revised: 12/2023
Document Id: 3c6c9b47-d0b2-499a-9cad-8e4bc9b1bdf6
Set id: 33dd2245-9abd-4b32-ac76-0f45a54c0f33
Version: 2
Effective Time: 20231215
 
Kramer Laboratories