Label: MINERAL OIL HEAVY- mineral oil liquid
- NDC Code(s): 82645-906-16, 82645-906-32
- Packager: Pharma Nobis, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 22, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
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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
- Keep out of reach of children
- Directions
- Inactive ingredient
- Other information
- CVS Label
- Leader Label
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INGREDIENTS AND APPEARANCE
MINERAL OIL HEAVY
mineral oil liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82645-906 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:82645-906-16 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/18/2018 2 NDC:82645-906-32 950 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/31/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 12/18/2018 Labeler - Pharma Nobis, LLC (118564114) Registrant - Pharma Nobis, LLC (118564114) Establishment Name Address ID/FEI Business Operations Pharma Nobis, LLC 118564114 manufacture(82645-906) , analysis(82645-906) , pack(82645-906) , label(82645-906)