Label: QUALITY CHOICE FIBER THERAPY- methylcellulose tablet
- NDC Code(s): 83324-228-01
- Packager: CHAIN DRUG MARKETING ASSOCIATION
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 7, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each caplet)
- Purpose
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Uses
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- relieves constipation (irregularity)
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- generally produces a bowel movement in 12 -72 hours.
Warnings
Choking: Taking this product without adequate fluid may cause it to swell and block your throat or esophagus and may cause choking. Do not take this product if you have difficulty in swallowing. If you experience chest pain, vomiting or difficulty in swallowing or breathing after taking this product, seek immediate medical attention.
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Directions
Take this product (child or adult dose) with at least 8 ounces (a full glass) of water or other fluid.
Taking this product without enough liquid may cause choking. See choking warning.
Age
Dose
Maximum Dose
adults & children 12 years of age and over
start with 2 caplets. Increase as needed up to 6 times per day.
Do not exceed 12 caplets per day
Children 6-11 years of age
Start with 1 caplet. Increase as needed up to 6 times per day
Do not exceed 6 caplets per day
children under 6 years of age
Consult a physician
Consult a physician
- Other information
- Inactive ingredients
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Principal Display Panel
QUALITY CHOICE®
NDC# 83324-228-01
Compare to Citrucel® Caplets Active Ingredients*
Fiber Therapy
Methylcellulose
- •
- Gentle and clinically proven effective†
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- Gives you additional fiber to help relieve occasional constipation
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- Fiber for irregularity that won’t cause excess gas††
- 100 Fiber Caplets
100% QC SATISFACTION GURANTEED
Distributed by CDMA, Inc. ©
Novi, MI 48375
Questions: 800-935-2362
*This product is not manufactured or distributed by GlaxoSmithKline, the distributor of CITRUCEL® Caplets.
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INGREDIENTS AND APPEARANCE
QUALITY CHOICE FIBER THERAPY
methylcellulose tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83324-228 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength METHYLCELLULOSE (4000 MPA.S) (UNII: MRJ667KA5E) (METHYLCELLULOSE (4000 MPA.S) - UNII:MRJ667KA5E) METHYLCELLULOSE (4000 MPA.S) 500 mg Inactive Ingredients Ingredient Name Strength ADIPIC ACID (UNII: 76A0JE0FKJ) CALCIUM CARBONATE (UNII: H0G9379FGK) CROSPOVIDONE (120 .MU.M) (UNII: 68401960MK) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYSORBATE 80 (UNII: 6OZP39ZG8H) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color ORANGE (Light orange) Score no score Shape CAPSULE (Caplet) Size 19mm Flavor Imprint Code RP122 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83324-228-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 09/20/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 09/20/2024 Labeler - CHAIN DRUG MARKETING ASSOCIATION (011920774)