Label: UP AND UP FIBER THERAPY- psyllium husk powder
- NDC Code(s): 11673-669-91
- Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 16, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient: (in each TEASPOON)
- Purpose
- Uses:
-
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.
Allergy alert:
This product may cause allergic reaction in people sensitive to inhaled or ingested psyllium.
Ask a doctor before use if you have
- ▪
- a sudden change in bowel habits persisting for 2 weeks
- ▪
- abdominal pain, nausea or vomiting
-
Directions:
Put one dose into an empty glass. Mix 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. Stir briskly and drink promptly. If mixture thickens, add more liquid and stir.
Adults 12 years & older:
1 rounded TEASPOON in 8 oz of liquid at the first sign of irregularity. Can be taken up to 3 times daily. Generally produces effect in 12 – 72 hours.
Children 6 – 11 yrs :
½ adult dose in 8 oz of liquid, up to 3 times daily
Children under 6 yrs:
Consult a doctor
Bulk forming fibers like psyllium husk may affect how well other medicines work. If you are taking a prescription medicine by mouth, take this product at least 2 hours before or 2 hours after the prescribed medicine. As your body adjusts to increased fiber intake, you may experience changes in bowel habits or minor bloating.
- Other information:
- Inactive ingredients:
-
PRINCIPAL DISPLAY PANEL
NDC 11673-669-91
Compare to active ingredient in Metamucil® 4 in 1 MultiHealth Fiber***
fiber therapy
100% natural psyllium husk
multi-benefit daily fiber supplement therapy for regularity
helps you feel less hungry between meals**
helps maintain healthy blood sugar levels as part of your diet**
helps lower cholesterol to promote heart health†
promotes digestive health**
sugar free
not a low calorie food
ORANGE FLAVOR 114 DOSES‡
FILL CONTROLLED BY WEIGHT NOT VOLUME
114 TEASPOON DOSES‡
NET WT 23.3 OZ (1.4 LB) 660 g
Naturally and Artificially Flavored
245 05 0216 R01 ID295403
Distributed by Target Corporation
Minneapolis, MN 55403
©2015 Target Brands, Inc.
Shop Target.com
GLUTEN FREE
**These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.
†See back for information about soluble fiber and heart disease
‡Serving size varies. See DIRECTIONS on back panel for more information
This product has a low glycemic index, a measure of the effect of dietary carbohydrates on blood sugar levels.
100% satisfaction guaranteed or your money back.
***This product is not manufactured or distributed by Procter & Gamble, owner of the registered trademark Metamucil ®.
-
INGREDIENTS AND APPEARANCE
UP AND UP FIBER THERAPY
psyllium husk powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-669 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PSYLLIUM HUSK (UNII: 0SHO53407G) (PSYLLIUM HUSK - UNII:0SHO53407G) PSYLLIUM HUSK 3.4 g in 5.79 g Inactive Ingredients Ingredient Name Strength aspartame (UNII: Z0H242BBR1) citric acid monohydrate (UNII: 2968PHW8QP) FD&C Yellow No. 6 (UNII: H77VEI93A8) maltodextrin (UNII: 7CVR7L4A2D) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color BROWN (Light yellowish) Score Shape Size Flavor ORANGE Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-669-91 660 g in 1 BOTTLE; Type 0: Not a Combination Product 10/26/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 10/26/2015 Labeler - Target Corporation (006961700)
