Label: CAREMOTION- sennosides tablet
-
Contains inactivated NDC Code(s)
NDC Code(s): 80415-004-01, 80415-004-02 - Packager: US Drugs Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated November 18, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- Purpose
- Uses
- Warnings
-
Directions
- take preferably at bedtime or as directed by a doctor
age
starting
dosage
maximum dosage
adults and children 12 years of age and over
2 tablets once a day
4 tablets twice a day
children 6 to under 12
years
1 tablet once a day
2 tablets twice a day
children 2 to under 6
years
1 /2 tablet once a day
1 tablet twice a day
children under 2 years
ask a doctor
ask a doctor
- Other information
- Inactive ingredients
- Questions or Comments? 1-866-561-2888
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CAREMOTION
sennosides tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80415-004 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES 8.6 mg Inactive Ingredients Ingredient Name Strength HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) CROSPOVIDONE (UNII: 2S7830E561) POVIDONE K30 (UNII: U725QWY32X) ISOPROPYL ALCOHOL (UNII: ND2M416302) MAGNESIUM STEARATE (UNII: 70097M6I30) METHYLENE CHLORIDE (UNII: 588X2YUY0A) Product Characteristics Color brown Score no score Shape ROUND Size 10mm Flavor Imprint Code CS Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80415-004-01 600 in 1 BOTTLE; Type 0: Not a Combination Product 06/14/2021 2 NDC:80415-004-02 800 in 1 BOTTLE; Type 0: Not a Combination Product 06/14/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 06/14/2021 Labeler - US Drugs Inc. (104282689) Registrant - US Drugs Inc. (104282689)
