Humco Castor Oil, USP (Regular)

Humco Castor Oil, USP (Regular)

Drug Labeling and Warnings

Drug Details


HUMCO CASTOR OIL (REGULAR)- castor oil liquid 
Humco Holding Group, Inc.

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.


Humco Castor Oil, USP (Regular)

Drug Facts

Active Ingredient

Castor Oil


Stimulant laxative


For the temporary relief of ocassional constipation. Bowel movement is generally produced in 6 to 12 hours.


Do not use when abdominal pain, nausea, or vomiting are present unless directed by a doctor.

Ask a doctor before use.

If you have noticed a sudden change in bowel habits that persists over a period of two weeks. Laxative products should not be used for a period of longer than 1 week unless directed by a doctor. Frequent or prolonged use may result in dependence on laxatives.

When using this product:

Discontinue use and consult a doctor if you have rectal bleeding or failure to have a bowel movement after the use of a laxative. These symptoms may indicate a serious condition.

If pregnant or breastfeeding ask a health professional before use.

Keep out of reach of children

In case of accidental overdose, seel professional assistance or contact a Poison Control Center immediately.


  • Adults and children 12 yrs. of age and older: 1 to 4 tablespoonfuls in a single day or as directed by a doctor.
  • Children 2 to under 12 years of age: 1 to 3 teasponfuls in a signle daily dose or as directed by a doctor.
  • Children under 2 yrs. of age: Consult a doctor before use.

Inactive Ingredient



image description

castor oil liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 0395-0513
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
water (UNII: 059QF0KO0R)  
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 0395-0513-94118 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2013
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33401/01/2013
Labeler - Humco Holding Group, Inc. (825672884)
NameAddressID/FEIBusiness Operations
Humco Holding Group, Inc.825672884manufacture(0395-0513) , analysis(0395-0513) , pack(0395-0513) , label(0395-0513)

Revised: 10/2017
Humco Holding Group, Inc.

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