Label: HUMCO MINERAL OIL HEAVY- mineral oil liquid
- NDC Code(s): 0395-1685-28
- Packager: Humco Holding Group, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 15, 2023
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Warnings
Do not take this product if you have abdominal pain, nausea, vomiting, change in bowel habits persisting more than 2 weeks, rectal bleeding or kidney failure are present, or use for a period of longer than 1 week unless directed by a doctor. Frequent or prolonged use may result in the dependence on laxatives.
Do not administer to infants or young children, bedridden or aged patients unless directed by a doctor.
- Ask a doctor before use if
- When using this Product discotinue use
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INGREDIENTS AND APPEARANCE
HUMCO MINERAL OIL HEAVY
mineral oil liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0395-1685 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINERAL OIL (UNII: T5L8T28FGP) (MINERAL OIL - UNII:T5L8T28FGP) MINERAL OIL 1000 mg in 1 mL Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0395-1685-28 3800 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/14/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 03/25/1998 Labeler - Humco Holding Group, Inc. (825672884) Registrant - Pharma Nobis, LLC (118564114) Establishment Name Address ID/FEI Business Operations Pharma Nobis, LLC 118564114 manufacture(0395-1685) , analysis(0395-1685) , pack(0395-1685) , label(0395-1685)