Night Time Cherry by Chain Drug Consortium, LLC / P & L Development, LLC Drug Facts

Night Time Cherry by

Drug Labeling and Warnings

Night Time Cherry by is a Otc medication manufactured, distributed, or labeled by Chain Drug Consortium, LLC, P & L Development, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NIGHT TIME CHERRY- dextromethorphan hydrobromide, doxylamine succinate syrup 
Chain Drug Consortium, LLC

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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Drug Facts

Active ingredients

Dextromethorphan HBr 15 mg
Doxylamine succinate 6.25 mg

Purpose

Cough suppressant
Antihistamine

Uses

temporarily relieves cold symptoms
cough runny nose and sneezing

Warnings

Do not use to make a child sleepy
if you are on a sodium-restricted diet
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 two 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 if you have

asthma emphysema glaucoma excessive phlegm (mucus) breathing problems chronic bronchitis
persistent or chronic cough cough associated with smoking trouble urinating due to enlarged prostate gland

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

you get nervous, dizzy or sleepless redness or swelling is present new symptoms occur
fever gets worse or lasts more than 3 days pain or cough gets worse or lasts more than 7 days
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 this and all drugs out of the reach of children.

In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately.

Directions

take only as recommended
use dosage cup or tablespoon (TBSP) do not exceed 4 doses per 24 hours
age dose
adults and children 12 years and over 2 tablespoons (30 mL) every 6 hours
children 4 years to under 12 years do not use unless directed by a doctor
children under 4 years do not use
When using Day Time and Night Time products, carefully read each label to ensure correct dosing.

Other Information

each tablespoon contains: sodium 18 mg store at controlled room temperature

Inactive ingredients

alcohol, blue 1, citric acid, flavors, high fructose corn syrup, polyethylene glycol, propylene glycol,
purified water, red 40, saccharin sodium, sodium citrate

Principal Display Panel

Premier Value

Night Time Cough Cherry all night cough relief

compare to the active ingredients in Vicks Nyquil Cough

Dextromethorphan HBr-cough suppressant

Doxylamine Succinate-Antihistamine

10% Alcohol

10 fl oz (296mL)

image of label
NIGHT TIME CHERRY 
dextromethorphan hydrobromide, doxylamine succinate syrup
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 68016-072
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE15 mg  in 15 mL
DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2) (DOXYLAMINE - UNII:95QB77JKPL) DOXYLAMINE SUCCINATE6.25 mg  in 15 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SACCHARIN SODIUM ANHYDROUS (UNII: I4807BK602)  
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
Product Characteristics
Color    Score    
ShapeSize
FlavorCHERRY (Cherry) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 68016-072-01296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/25/200912/31/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34108/25/200912/31/2019
Labeler - Chain Drug Consortium, LLC (101668460)
Registrant - P & L Development, LLC (800014821)

Revised: 12/2018
 
Chain Drug Consortium, LLC