Label: MEIJER ADULT MUCUS PLUS CHEST CONGESTION- guaifenesin syrup
- NDC Code(s): 79481-7430-8
- Packager: MEIJER DISTRIBUTION, INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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.
Drug Label Information
Updated April 19, 2023
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- Active ingredient (in each 10 mL)
- Purpose
- Uses
-
Warnings
Ask a doctor before use if you have
- ▪
- cough that occurs with too much phlegm (mucus)
- ▪
- cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema
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Directions
- ▪
- do not take more than 6 doses in any 24-hour period
- ▪
- measure only with dosing cup provided
- ▪
- keep dosing cup with product
- ▪
- mL = milliliter
- ▪
- this adult product is not intended for use in children under 12 years of age
age
dose
adults and children 12 years and over
10 ml – 20 ml every 4 hours
children under 12 years
do not use
- Other information
- Inactive ingredients
- Questions or comments
-
Principal Display Panel
NDC# 79481-7430-8
COMPARE TO THE ADULT ROBITUSSIN MUCUS + CHEST CONGESTION ACTIVE INGREDIENT*
Meijer
ADULT
For Ages 12 & Over
Mucus+Chest
Congestion
Guaifenesin (Expectorant)
Relieves:
- •
- Mucus
- •
- Chest congestion
Sugar-Free
No Added Alcohol
Use Dosage Cup Included
Natural Cherry Flavor
8 FL OZ (237 mL)
IMPORTANT: Keep this carton for future reference on full labeling.
*This product is not manufactured or distributed by Pfizer, owner of the registered trademark Adult Robitussin® Mucus + Chest Congestion.
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INGREDIENTS AND APPEARANCE
MEIJER ADULT MUCUS PLUS CHEST CONGESTION
guaifenesin syrupProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79481-7430 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 200 mg in 10 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) EDETATE DISODIUM (UNII: 7FLD91C86K) FD&C RED NO. 40 (UNII: WZB9127XOA) GLYCERIN (UNII: PDC6A3C0OX) 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 RED Score Shape Size Flavor CHERRY (Naturally and Artificially) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79481-7430-8 1 in 1 CARTON 03/31/2023 1 237 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 final part341 03/31/2023 Labeler - MEIJER DISTRIBUTION, INC (006959555)