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GNP Castor Oil

Dosage form: liquid
Ingredients: CASTOR OIL 1mg in 1mL
Labeler: Amerisource Bergen
NDC Code: 24385-515

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.

GNP Castor Oil

Drug Facts

Active Ingredient

Castor Oil


Stimulant Laxative


For the temporary relief of occasional 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 2 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 the 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. Thee symptoms may indicate a serious condition.

If pregnant or breast feeding

ask a health professional before use

Keep out of reach of children.

In case of accidental overdose, seek profssional assistance or contact a Poison Control Center immediately.


Preferably take on an empty stomach. May be taken with juice to improve taste.

Adults and children 12 yrs. of age and older: 1 to 4 tablesponfuls in a single daily dose or as directed by a doctor.

Children 2 to under 12 yrs. of age: 1 to 3 teaspoonfuls in a single dose or as directed by a doctor.

Children under 2 yrs. of age: Consult a doctor before use.


Do not use if Taper Evident Seal is broken or missing. This product is sealed with either a shrink band around cap imprinted "Sealed For your Protection" or foil seal under cap.

Other Information

storage. Keep tightly closed and away from excessive heat.

Inactive Ingredient



castor oil liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24385-515
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:24385-515-30177 mL in 1 BOTTLE, PLASTIC
2NDC:24385-515-4659 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33401/01/2008
Labeler - Amerisource Bergen (007914906)
Registrant - Humco Holding Group, Inc (825672884)
Humco Holding Group, Inc.825672884analysis(24385-515), pack(24385-515), manufacture(24385-515), label(24385-515)

Amerisource Bergen

Medically reviewed on Nov 2, 2017

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.