Label: DERMAPHOR- skin protectant ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 61924-184-04, 61924-184-08, 61924-184-16 - Packager: DermaRite Industries, LLC
- 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 January 17, 2020
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- DermaPhor Package Label and Principal Display Panel
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INGREDIENTS AND APPEARANCE
DERMAPHOR
skin protectant ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61924-184 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 44 g in 100 g Inactive Ingredients Ingredient Name Strength MINERAL OIL (UNII: T5L8T28FGP) LANOLIN ALCOHOLS (UNII: 884C3FA9HE) PARAFFIN (UNII: I9O0E3H2ZE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61924-184-04 106 g in 1 TUBE; Type 0: Not a Combination Product 11/17/2016 2 NDC:61924-184-08 198 g in 1 TUBE; Type 0: Not a Combination Product 11/17/2016 3 NDC:61924-184-16 454 g in 1 JAR; Type 0: Not a Combination Product 11/17/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 11/17/2016 Labeler - DermaRite Industries, LLC (883925562) Registrant - DermaRite Industries, LLC (883925562) Establishment Name Address ID/FEI Business Operations DermaRite Industries, LLC 883925562 manufacture(61924-184)