Label: LANODERM- otc skin protectant drug products ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 61924-232-04, 61924-232-05, 61924-232-15 - Packager: Dermarite Industries LLC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated September 14, 2018
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INGREDIENTS AND APPEARANCE
LANODERM
otc skin protectant drug products ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61924-232 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LANOLIN (UNII: 7EV65EAW6H) (LANOLIN - UNII:7EV65EAW6H) LANOLIN 0.3 g in 100 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) MINERAL OIL (UNII: T5L8T28FGP) WHITE WAX (UNII: 7G1J5DA97F) LANOLIN ALCOHOLS (UNII: 884C3FA9HE) PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO) WATER (UNII: 059QF0KO0R) SODIUM BORATE (UNII: 91MBZ8H3QO) SODIUM CHLORIDE (UNII: 451W47IQ8X) EDETATE DISODIUM (UNII: 7FLD91C86K) DMDM HYDANTOIN (UNII: BYR0546TOW) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61924-232-04 113 g in 1 TUBE; Type 0: Not a Combination Product 04/16/2012 2 NDC:61924-232-05 5 g in 1 PACKET; Type 0: Not a Combination Product 04/16/2012 3 NDC:61924-232-15 15 g in 1 PACKET; Type 0: Not a Combination Product 04/16/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 04/16/2012 Labeler - Dermarite Industries LLC (883925562) Registrant - DermaRite Industries, LLC (883925562) Establishment Name Address ID/FEI Business Operations Dermarite Industries LLC 883925562 manufacture(61924-232)