Label: MINERAL OIL liquid
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- NDC Code(s): 0363-0831-43
- Packager: Walgreen Co
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated March 30, 2021
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use
- Do not use
- Ask a doctor before use if you have
- Ask a doctor or pharmacist before use if you are
- When using this product
- Stop use ad ask a doctor
- If breast feeding
- Keep out of reach of children.
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Directions
- do not take with meals
- take only at bedtime
- may be taken as a single daily dose or in divided doses
adults and children 12 years of age and over - 1 to 3 Tablespoons (15 - 45 mL) maximum 3 Tablespoons (45 mL) in 24 hours
children 6 to under 12 years of age - 1 to 3 teaspoons (5 - 15 mL) maximum 3 teaspoons (15 mL) in 24 hours
children under 6 years of age - do not use, consult a doctor
- Other information
- Inactive ingredients
- adverse reaction
-
principal display panel
Well at
Walgreens
WLAGREENS PHARMACST RECOMMENDED
INTESTINAL LUBRICANT
Mineral Oil
Lubricant Lazative
- For relief of occaskonal constipation
- Tasteless
- Odorless
- Colorles
16 FL OZ (1 PT) 473 mL
Walgrees Pharmacist Survey Study, November 2012
TAMPER EVIDENT: DO NOT USE IF THE UNDER CAP PRINTED SAFETY FOIL IS BROKEN OR MISSING
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INGREDIENTS AND APPEARANCE
MINERAL OIL
mineral oil liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0831 Route of Administration ORAL, TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINERAL OIL (UNII: T5L8T28FGP) (MINERAL OIL - UNII:T5L8T28FGP) MINERAL OIL 999 mg in 1 mL Inactive Ingredients Ingredient Name Strength TOCOPHEROL (UNII: R0ZB2556P8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0831-43 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/16/1994 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 06/16/1994 Labeler - Walgreen Co (008965063) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(0363-0831)