Label: IBO- mineral oil liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 82677-0002-1 - Packager: Elgoalin Bio Co.,Ltd
- Category: HUMAN OTC 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 April 25, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
IBO
mineral oil liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82677-0002 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINERAL OIL (UNII: T5L8T28FGP) (MINERAL OIL - UNII:T5L8T28FGP) MINERAL OIL 55 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82677-0002-1 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/18/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/18/2022 Labeler - Elgoalin Bio Co.,Ltd (688353068) Registrant - Elgoalin Bio Co.,Ltd (688353068) Establishment Name Address ID/FEI Business Operations Elgoalin Bio Co.,Ltd 688353068 manufacture(82677-0002)
