Purpose
- Laxative
The following Structured Product Label (SPL) was submitted to the FDA by Us Drugs Inc. for the product Caremotion (NDC 80415-004). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding purpose, uses, do not use, ask a doctor before use if you have, stop use and ask a doctor if, if pregnant or breast-feeding,, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
you have rectal bleeding or fail to have a bowel movement after use of a laxative. These may indicate a serious condition.
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)
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 |
■ each tablet contains: calcium 5 mg
■ store at 20-25°C (68-77°F); excursions permitted between 15°-30°C (59°-86°F)
crospovidone, dichloromethane, hypromellose, isopropyl alcohol, lactose, magnesium stearate, microcrystalline cellulose, povidone
*This product is not manufactured or distributed by Purdue Products L.P., owner of the registered trademark Senokot
Distributed by:
US Drugs Inc.
11380 7th Street, Rancho Cucamonga, CA 91730, USA
Country of Origin: India
* Please review the disclaimer below.