Label: CDMA FIBER THERAPY- methylcellulose tablet
- NDC Code(s): 63868-166-10
- Packager: CHAIN DRUG MARKETING ASSOCIATION
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 18, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each caplet)
- Purpose
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Uses
- helps restore and maintain regularity
- relieves constipation (irregularity)
- for constipation associated with other bowel disorders like IBS when recommended by a doctor.
- 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# 63868-166-10
Compare to Citrucel ®Caplets Active Ingredients*
Fiber Therapy
Fiber Therapy for Regularity
Methylcellulose
- 100% non-allergenic
- Gentle and Gluten-Free
- 100 CAPLETS
100% QC SATISFACTION GURANTEED
Distributed by C.D.M.A., Inc. ©
43157 W. Nine Mile
Novi, MI 48376-0995
Questions: 248-449-9300
*This product is not manufactured or distributed by GlaxoSmithKline, the distributor of CITRUCEL® Caplets.
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INGREDIENTS AND APPEARANCE
CDMA FIBER THERAPY
methylcellulose tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-166 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) MALTODEXTRIN (UNII: 7CVR7L4A2D) 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:63868-166-10 100 in 1 BOTTLE; Type 0: Not a Combination Product 04/19/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 04/19/2019 Labeler - CHAIN DRUG MARKETING ASSOCIATION (011920774)