Label: PURE BABY DIAPER RASH- zinc oxide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 59886-414-32 - Packager: Fischer Pharmaceuticals Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 December 28, 2017
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- SPL UNCLASSIFIED SECTION
- Active Ingredients
- Purpose
- Uses
- Warnings
- Directions
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Inactive Ingredients
Bisabolol, Calendula Officinalis Flower Extract, Caprylic/Capric Triglyceride, Coco-Caprylate, Dunaliella Salina Extract, Ethylhexylglycerin, Globularia Alypum Leaf Extract, Glycerin, Helianthus Annuus (Sunflower) Seed Oil, Hydrogenated Castor Oil, Magnesium Sulfate, Olea Europaea (Olive) Fruit Oil, Phenoxyethanol, Polyglyceryl-2 Dipolyhydroxystearate, Polyglyceryl-3 Diisostearate, Potassium Sorbate, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Sodium Benzoate, Tocopherol, Water.
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- PRINCIPAL DISPLAY PANEL - 113 g Tube Label
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INGREDIENTS AND APPEARANCE
PURE BABY DIAPER RASH
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59886-414 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide 40 g in 100 g Inactive Ingredients Ingredient Name Strength LEVOMENOL (UNII: 24WE03BX2T) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) Coco-Caprylate (UNII: 4828G836N6) DUNALIELLA SALINA (UNII: F4O1DKI9A6) Ethylhexylglycerin (UNII: 147D247K3P) GLOBULARIA CORDIFOLIA WHOLE (UNII: SD327VQ78H) Glycerin (UNII: PDC6A3C0OX) SUNFLOWER OIL (UNII: 3W1JG795YI) Hydrogenated Castor Oil (UNII: ZF94AP8MEY) MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I) OLIVE OIL (UNII: 6UYK2W1W1E) Phenoxyethanol (UNII: HIE492ZZ3T) Polyglyceryl-2 Dipolyhydroxystearate (UNII: 9229XJ4V12) Polyglyceryl-3 Diisostearate (UNII: 46P231IQV8) Potassium Sorbate (UNII: 1VPU26JZZ4) ALMOND OIL (UNII: 66YXD4DKO9) Sodium Benzoate (UNII: OJ245FE5EU) Tocopherol (UNII: R0ZB2556P8) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59886-414-32 113 g in 1 TUBE; Type 0: Not a Combination Product 01/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part347 01/01/2018 Labeler - Fischer Pharmaceuticals Ltd (600158976) Establishment Name Address ID/FEI Business Operations Fischer Pharmaceuticals Ltd 600410514 MANUFACTURE(59886-414)