Label: PREMIER VALUE- mineral oil
- NDC Code(s): 68016-831-43
- Packager: Pharmacy Value Alliance LLC
- 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 11, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- 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 and ask a doctor
- If breast feeding,
- Keep out of reach of children
-
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
- Questions?
-
Adverse Reaction
Distributed by: Pharmacy Value Alliance LLC
407 East Lancaster Avenue, Wayne, PA 19087 www.emersongroup.com
If for any reason you are not satisfied with this product,
please return it to the store where purchased for a full refund.
- principal display panel
-
INGREDIENTS AND APPEARANCE
PREMIER VALUE
mineral oilProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68016-831 Route of Administration ORAL 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:68016-831-43 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/19/2009 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 05/19/2009 Labeler - Pharmacy Value Alliance LLC (101668460) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(68016-831) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(68016-831)
