TARGET CHILDRENS DT AND NT COLD AND COUGH- brompheniramine maleate,dextromethorphan hbr,phenylephrine hcl,diphenhydramine hcl, phenylephrine hcl 
TARGET CORPORATION

----------

TARGET Children’s Daytime & Nighttime Value Pack Drug Facts

Children’s Daytime Cold & Cough
Active ingredients (in each 10 mL)

Brompheniramine maleate, 2 mg

Dextromethorphan HBr, 10 mg

Phenylephrine HCl, 5 mg

Children’s NighttimeCold & Congestion
Active ingredients (in each 10 mL)

Diphenhydramine HCL12.5 mg

Phenylephrine HCL5 mg

Purposes forChildren’s Daytime Cold & Cough

Antihistamine

Cough suppressant

Nasal decongestant

Purposes forChildren’s NighttimeCold & Congestion

Antihistamine/Cough suppressant

Nasal decongestant

Uses

Daytime

Nighttime

Warnings Do not use

Daytime

Nighttime only

Ask a doctor before use if you have

DAYTIME

  • heart disease
  • high blood pressure
  • diabetes
  • thyroid disease
  • trouble urinating due to an enlarged prostate gland
  • glaucoma
  • cough that occurs with too much phlegm (mucus)
  • a breathing problem or chronic cough that lasts such as occurs with smoking, asthma, chronic bronchitis, or emphysema.

NIGHTTIME

  • heart disease
  • high blood pressure
  • diabetes
  • thyroid disease
  • trouble urinating due to an enlarged prostate gland
  • glaucoma
  • cough that occurs with too much phlegm (mucus)
  • a breathing problem or chronic cough that lasts such as occurs with smoking, asthma, chronic bronchitis, or emphysema.

Ask a doctor or pharmacist before use if you are

DAYTIME

  • taking any other oral nasal decongestant or stimulant
  • taking sedatives or tranquilizers

NIGHTTIME

  • taking any other oral nasal decongestant or stimulant
  • taking sedatives or tranquilizers

When using this product

Daytime

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

Nighttime

  • do not use more than directed.
  • may cause marked drowsiness
  • avoid 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

DAYTIME

  • nervousness, dizziness, or sleeplessness occur
  • symptoms do not get better with 7 days or are accompanied with fever
  • cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or headache.

These could be signs of a serious condition.

NIGHTTIME

  • nervousness, dizziness, or sleeplessness occur
  • symptoms do not get better with 7 days or are accompanied with fever
  • cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or headache.

These could be signs of a serious condition.

Keep out of reach of children.

Daytime

In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Nighttime

In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

If pregnant or breast-feeding,

Ask a health professional before use

Directions

Daytime

age

dose

Adults and children 12 years and over

20 mL every 4 hours

children 6 to under 12 years

10 mL every 4 hours

children under 6 years of age

do not use


Nighttime

age

dose

 Adults and children 12 years and over

 20 mL every 4 hours

 children 6 to under 12 years

10 mL every 4 hours

 children under 6 years of age

do not use

Other information

Daytime

Nighttime

Inactive ingredients

Inactive ingredients for Day Time 

anhydrous citric acid, FD&C blue #1, FD&C red #40, flavor, glycerin, propyl gallate, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose

Inactive ingredients for Nighttime 

anhydrous citric acid, FD&C blue #1, FD&C red #40, flavor, glycerin, propyl gallate, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose

Questions or comments?

1-866-467-2748

Principal Display Panel

Compare to the active ingredients in Children's Dimetapp® Cold & Cough*

Children's Daytime

Cold & Cough

Brompheniramine Maleate 2 mg (Antihistamine),

Dextromethorphan HBr 10 mg (Cough Suppressant)

Phenylephrine HCI 5 mg (Nasal Decongestant)

Dosing Cup Included

Ages 6+ Years

Grape Flavor

NATURALLY AND ARTIFICIALLY FLAVORED

4 FL OZ (118mL)

Compare to the active ingredients in Children's Dimetapp® Nighttime Cold & Congestion**

Children's Nighttime

Cold & Congestion

Diphenhydramine HCI 12.5 mg (Antihistamine / Cough Suppressant)

Phenylephrine HCI 5 mg (Nasal Decongestant)

Dosing Cup Included

Ages 6+ Years

Grape Flavor

NATURALLY AND ARTIFICIALLY FLAVORED

4 FL OZ (118mL)

8 FL OZ (236 mL) TOTAL

DO NOT TAKE BOTH PRODUCTS AT THE SAME TIME. ALWAYS WAIT AT LEAST 4 HOURS BEFORE TAKING ANOTHER DOSE OF THE PRODUCT.

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL AROUND BOTTLE OR UNDER CAP IS BROKEN OR MISSING

IMPORTANT:KEEP THIS CARTON FOR FUTURE REFERENCE FOR FULL LABELING

*This product is not manufactured or distributed by Foundation Consumer Brands, LLC, the distributor of Children's Dimetapp® Cold & Congestion.

Satisfaction guaranteed – Love it or your money back

We welcome any questions you may have at

Target.com/comments

Or 1-800-910-6874.

Distributed by: Target Corporation

Minneapolis, MN 55403

Made in the U.S.A. with domestic and imported ingredients

TM & ©2024 Target Brands, Inc,

Product Label

TARGET Children's Daytime & Nightime Cold & Cough Value pack
TARGET CHILDRENS DT AND NT COLD AND COUGH 
brompheniramine maleate,dextromethorphan hbr,phenylephrine hcl,diphenhydramine hcl, phenylephrine hcl kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82442-536
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82442-536-081 in 1 KIT; Type 0: Not a Combination Product06/14/2024
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 BOTTLE, PLASTIC 118 mL
Part 21 BOTTLE, PLASTIC 118 mL
Part 1 of 2
TGT CHILDRENS DAYTIME COLD AND COUGH 
brompheniramine maleate, dextromethorphan hbr,phenylephrine hcl liquid
Product Information
Item Code (Source)NDC:82442-464
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BROMPHENIRAMINE MALEATE (UNII: IXA7C9ZN03) (BROMPHENIRAMINE - UNII:H57G17P2FN) BROMPHENIRAMINE MALEATE2 mg  in 10 mL
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 10 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYL GALLATE (UNII: 8D4SNN7V92)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
Product Characteristics
ColorpurpleScore    
ShapeSize
FlavorGRAPEImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82442-464-04118 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 DrugM01206/14/2024
Part 2 of 2
TGT CHILDRENS NIGHTTIME COLD AND COUGH 
diphenhydramine hcl,phenylephrine hcl liquid
Product Information
Item Code (Source)NDC:82442-466
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE12.5 mg  in 10 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYL GALLATE (UNII: 8D4SNN7V92)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
Product Characteristics
ColorpurpleScore    
ShapeSize
FlavorGRAPEImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82442-466-04118 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 DrugM01206/14/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01206/14/2024
Labeler - TARGET CORPORATION (006961700)

Revised: 11/2025
Document Id: 42d76401-ab6f-17d5-e063-6394a90a8718
Set id: 05ac2a40-5eee-4013-b55b-6e370a28b21c
Version: 3
Effective Time: 20251105
 
TARGET CORPORATION