Label: STOP THE DIARRHEA- kaolin liquid
- NDC Code(s): 86173-814-02, 86173-814-06, 86173-814-12
- Packager: Click Industries LLC
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated March 15, 2024
If you are a consumer or patient please visit this version.
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- DRUG FACTS
- Active Ingredient per Teaspoon:
- Purpose
- Uses:
- WARNINGS:
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Directions:
Shake well before using. Apply directly into your pet's mouth or mix into food every 12 hours or as recommended by a veterinarian. Consult a veterinarian for use of this product on pets less than 5 LB. Individual results may vary.
Pet Weight Dosage 5-15LB (1-6.8 kg) 1 tsp (5 ml) 16-50LB (7.3-22.7 kg) 2 tsp (10 ml) Over 50LB (22.7 kg) 1 tbsp (15 ml) - Inactive Ingredients:
- Storage:
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SPL UNCLASSIFIED SECTION
MADE IN THE USA*
RELIEVE IRRITATION & DISCOMFORT
PROVIDES UPSET STOMACH RELIEF
HELPS FIRM LOOSE STOOL
KAOLIN ABSORBS TOXINS & BACTERIA
FOR DOGS
NOT INTENDED FOR HUMAN USE.
Keep out of reach of children and pets to avoid unintended consumption. Use with care and follow instructions closely.
DO NOT USE IF PRODUCT APPEARS TO BE TAMPERED WITH OR SEAL IS BROKEN
STORE AT ROOM TEMPERATURE. DO NOT EXPOSE TO EXCESSIVE HEAT OR MOISTURE
Manufactured For:
Chew + Heal
Surfside, FL
www.chewandheal.com
*MADE IN U.S.A. with globally sourced ingredients - Packaging
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INGREDIENTS AND APPEARANCE
STOP THE DIARRHEA
kaolin liquidProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:86173-814 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength KAOLIN (UNII: 24H4NWX5CO) (KAOLIN - UNII:24H4NWX5CO) KAOLIN 8 g in 100 mL Inactive Ingredients Ingredient Name Strength CALCIUM (UNII: SY7Q814VUP) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT) MAGNESIUM (UNII: I38ZP9992A) PECTIN (UNII: 89NA02M4RX) POTASSIUM (UNII: RWP5GA015D) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CHLORIDE (UNII: 451W47IQ8X) SORBIC ACID (UNII: X045WJ989B) SORBITOL (UNII: 506T60A25R) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:86173-814-02 59 mL in 1 BOTTLE 2 NDC:86173-814-06 177 mL in 1 BOTTLE 3 NDC:86173-814-12 355 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/01/2024 Labeler - Click Industries LLC (117033580)