Label: END-ITCH FOR ECZEMA cream
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Contains inactivated NDC Code(s)
NDC Code(s): 60858-315-03 - Packager: Crystal Connections, LLC
- Category: HUMAN OTC DRUG LABEL
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 May 15, 2015
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- OTC - ACTIVE INGREDIENT
- INACTIVE INGREDIENTS
- OTC - KEEP OUT OF REACH OF CHILDREN SECTION
- WARNINGS
- OTC - PURPOSE SECTION
- OTC - STOP USE SECTION
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
END-ITCH FOR ECZEMA
end-itch for eczema creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60858-315 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y) OATMEAL 0.24 g in 1 mL Inactive Ingredients Ingredient Name Strength ALMOND OIL (UNII: 66YXD4DKO9) YELLOW WAX (UNII: 2ZA36H0S2V) JOJOBA OIL (UNII: 724GKU717M) lanolin (UNII: 7EV65EAW6H) rosemary (UNII: IJ67X351P9) ALPHA-TOCOPHEROL (UNII: H4N855PNZ1) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60858-315-03 94 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/15/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 05/15/2015 Labeler - Crystal Connections, LLC (016582119) Establishment Name Address ID/FEI Business Operations American Pharmaceuticals and Cosmetics, Inc. 038023805 manufacture(60858-315)