Label: CITRUCEL- methylcellulose tablet
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NDC Code(s):
0135-0199-01,
0135-0199-02,
0135-0199-06,
0135-0199-07, view more0135-0199-08, 0135-0199-09
- Packager: Haleon US Holdings LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 5, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each caplet)
- Purpose
- Uses
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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.
Ask a doctor before use if you have
- •
- a sudden change in bowel habits that persists for two weeks
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- abdominal pain, nausea or vomiting
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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
- Questions or comments?
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Additional information found on label
TAMPER EVIDENT PACKAGE
BOTTLE SEALED WITH PRINTED FOIL UNDER CAP.
DO NOT USE IF FOIL IS MISSING OR BROKEN.
Distributed by:
GSKConsumer Healthcare
Warren, NJ 07059
*When Used As Directed.
**Based On Laboratory Testing.
Individual Results May Vary.
Trademarks are owned by or licensed to the GSK group of companies
©2018 GSK or its licensor.
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
CITRUCEL
methylcellulose tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0135-0199 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 CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561) ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) SODIUM LAURYL SULFATE (UNII: 368GB5141J) Product Characteristics Color orange Score no score Shape FREEFORM (Caplet) Size 19mm Flavor Imprint Code CIT Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0135-0199-01 180 in 1 BOTTLE; Type 0: Not a Combination Product 02/01/2010 2 NDC:0135-0199-02 100 in 1 BOTTLE; Type 0: Not a Combination Product 02/01/2010 3 NDC:0135-0199-06 2 in 1 POUCH; Type 0: Not a Combination Product 02/01/2010 4 NDC:0135-0199-07 240 in 1 BOTTLE; Type 0: Not a Combination Product 02/01/2010 5 NDC:0135-0199-08 50 in 1 CARTON 02/01/2010 5 NDC:0135-0199-06 2 in 1 POUCH; Type 0: Not a Combination Product 6 NDC:0135-0199-09 1 in 1 PACKAGE 02/15/2017 6 240 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 M007 02/01/2010 Labeler - Haleon US Holdings LLC (079944263)