Label: CHILDRENS MUCUS RELIEF CHEST CONGESTION- guaifenesin solution
- NDC Code(s): 63868-770-04
- Packager: Chain Drug Manufacturing Assn
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 18, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each 5 mL)
- Purpose
- Uses
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Warnings
Ask a doctor before use if the child has
- ▪
- cough that occurs with too much phlegm (mucus)
- ▪
- persistent or chronic cough such as occurs with asthma
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Directions
- ▪
- do not take more than 6 doses in any 24-hour period
- ▪
- measure only with dosing cup provided
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- do not use dosing cup with other products
- ▪
- mL = milliliter
Age Dose children 6 years to under 12 years
5 mL – 10 mL every 4 hours
children 4 years to under 6 years
2.5 mL – 5 mL every 4 hours
children under 4 years
do not use
- Other information
- Inactive ingredients
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PRINCIPAL DISPLAY PANEL - 118 mL Bottle Carton
QC QUALITY CHOICE NDC 63868-770-04
Children's
Mucus reliefExpectorant
Guaifenesin
Oral Solution, USP
Each Dose of Grape Flavored
Children’s Mucus Relief:
Relieves Chest Congestion
- Breaks up Mucus
Alcohol Free- See New Dosing Information
Grape
Flavor4 FL OZ
(118 mL)IMPORTANT:
Keep this carton for future reference on full labeling.
DOSAGE CUP INCLUDED
*This product is not manufactured or distributed by Reckitt Benckiser, distributor of Children’s Mucinex.®
Distributed by C.D.M.A.,Inc©
43157 W. Nine Mile
Novi, MI 48376-0995
Questions: 248-449-9300
QC 100% Satisfaction Guaranteed.
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INGREDIENTS AND APPEARANCE
CHILDRENS MUCUS RELIEF CHEST CONGESTION
guaifenesin solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-770 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Guaifenesin (UNII: 495W7451VQ) (Guaifenesin - UNII:495W7451VQ) Guaifenesin 100 mg in 5 mL Inactive Ingredients Ingredient Name Strength anhydrous citric acid (UNII: XF417D3PSL) EDETATE DISODIUM (UNII: 7FLD91C86K) FD&C blue no. 1 (UNII: H3R47K3TBD) FD&C red no. 40 (UNII: WZB9127XOA) POTASSIUM CITRATE (UNII: EE90ONI6FF) propylene glycol (UNII: 6DC9Q167V3) water (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) SORBITOL (UNII: 506T60A25R) sucralose (UNII: 96K6UQ3ZD4) xanthan gum (UNII: TTV12P4NEE) 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:63868-770-04 1 in 1 CARTON 10/19/2015 1 118 mL in 1 BOTTLE; 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 10/19/2015 Labeler - Chain Drug Manufacturing Assn (011920774)