Label: BABY OIL- glycerin oil solution
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Contains inactivated NDC Code(s)
NDC Code(s): 71538-006-01 - Packager: NANONATURE
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated July 17, 2017
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BABY OIL
glycerin oil solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71538-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) Glycerin 11 g in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Olive Oil (UNII: 6UYK2W1W1E) Retinol (UNII: G2SH0XKK91) Tocopherol (UNII: R0ZB2556P8) Ascorbic Acid (UNII: PQ6CK8PD0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71538-006-01 100 mL in 1 PACKAGE; Type 0: Not a Combination Product 07/17/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/17/2017 Labeler - NANONATURE (689851291) Registrant - NANONATURE (689851291) Establishment Name Address ID/FEI Business Operations NANONATURE 689851291 manufacture(71538-006)