TARGET CHILDRENS DT AND NT COLD AND COUGH- brompheniramine maleate,dextromethorphan hbr,phenylephrine hcl,diphenhydramine hcl, phenylephrine hcl kit
TARGET CHILDRENS DT AND NT COLD and COUGH by
Drug Labeling and Warnings
TARGET CHILDRENS DT AND NT COLD and COUGH by is a Otc medication manufactured, distributed, or labeled by TARGET CORPORATION. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
- Children’s Daytime Cold & Cough Active ingredients (in each 10 mL)
- Children’s Nighttime Cold & Congestion Active ingredients (in each 10 mL)
- Purposes for Children’s Daytime Cold & Cough
- Purposes for Children’s Nighttime Cold & Congestion
-
Uses
Daytime
- ▪
temporarily relieves
- ▪ nasal congestion
- ▪ runny nose
- ▪ cough
- ▪ sneezing
- ▪ itching of the nose or throat
- ▪ itchy, watery eyes due to hay fever
- ▪ temporarily restores freer breathing through the nose.
Nighttime
- ▪
temporarily relieves
- ▪ nasal congestion
- ▪ runny nose
- ▪ cough
- ▪ sneezing
- ▪ itching of the nose or throat
- ▪ itchy, watery eyes due to hay fever
- ▪ temporarily restores freer breathing through the nose.
- ▪
temporarily relieves
-
Warnings Do not use
Daytime
- ▪ to sedate a child or to make a child sleepy
- ▪ 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 child's prescription drug contains an MAOI, ask a doctor or pharmacist before giving this product.
Nighttime only
- ▪ to sedate a child or to make a child sleepy
- ▪ 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 child's prescription drug contains an MAOI, ask a doctor or pharmacist before giving this product.
- ▪ With any other product containing diphenhydramine, even one used on skin
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.
- If pregnant or breast-feeding,
-
Directions
Daytime
- ▪ do not take more than 6 doses in any 24-hour period
- ▪ measure only with dosing cup provided.
- ▪ Keep dosage cup with product
- ▪ mL= milliliter
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- ▪ do not take more than 6 doses in any 24-hour period
- ▪ measure only with dosing cup provided.
- ▪ Keep dosage cup with product
- ▪ mL= milliliter
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
-
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?
-
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)
- Sneezing, stuffy or runny nose, cough, itchy or watery eyes
- No added alcohol
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)
- Sneezing, stuffy or runny nose, cough, itchy or watery eyes
- No added alcohol
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
-
INGREDIENTS AND APPEARANCE
TARGET CHILDRENS DT AND NT COLD AND COUGH
brompheniramine maleate,dextromethorphan hbr,phenylephrine hcl,diphenhydramine hcl, phenylephrine hcl kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 82442-536 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 82442-536-08 1 in 1 KIT; Type 0: Not a Combination Product 06/14/2024 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE, PLASTIC 118 mL Part 2 1 BOTTLE, PLASTIC 118 mL Part 1 of 2 TGT CHILDRENS DAYTIME COLD AND COUGH
brompheniramine maleate, dextromethorphan hbr,phenylephrine hcl liquidProduct Information Item Code (Source) NDC: 82442-464 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BROMPHENIRAMINE MALEATE (UNII: IXA7C9ZN03) (BROMPHENIRAMINE - UNII:H57G17P2FN) BROMPHENIRAMINE MALEATE 2 mg in 10 mL DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 10 mg in 10 mL PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 5 mg in 10 mL Inactive Ingredients Ingredient Name Strength 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 Color PURPLE Score Shape Size Flavor GRAPE Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 82442-464-04 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 06/14/2024 Part 2 of 2 TGT CHILDRENS NIGHTTIME COLD AND COUGH
diphenhydramine hcl,phenylephrine hcl liquidProduct Information Item Code (Source) NDC: 82442-466 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 12.5 mg in 10 mL PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 5 mg in 10 mL Inactive Ingredients Ingredient Name Strength 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 Color PURPLE Score Shape Size Flavor GRAPE Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 82442-466-04 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 06/14/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 06/14/2024 Labeler - TARGET CORPORATION (006961700)
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