Label: PERIGUARD- otc skin protectant drug products ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 61924-205-04, 61924-205-05, 61924-205-07, 61924-205-15 - 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 13, 2022
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- Active Ingredient:
- Purpose:
- Uses:
- Warnings:
- Warnings:
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- Other Information:
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Inactive Ingredients:
Water, Lanolin, Mineral Oil, Paraffin, Zinc Oxide, Sorbitan Sequioleate, Beeswax, Propylene Glycol, Imidazolidinyl Urea, Methylparaben,propylparaben, Aluminum Stearate, Phenoxyethanol, Fragrance, Chloroxylenol,Cholecalciferol, Retinyl Palmitate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Zea Mays (corn) Oil
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INGREDIENTS AND APPEARANCE
PERIGUARD
otc skin protectant drug products ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61924-205 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 49.9 g in 100 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) ALUMINUM STEARATES (UNII: O4D7U3B46U) WHITE WAX (UNII: 7G1J5DA97F) CORN OIL (UNII: 8470G57WFM) CHOLECALCIFEROL (UNII: 1C6V77QF41) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) CHLOROXYLENOL (UNII: 0F32U78V2Q) IMIDUREA (UNII: M629807ATL) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) LANOLIN (UNII: 7EV65EAW6H) MINERAL OIL (UNII: T5L8T28FGP) PARAFFIN (UNII: I9O0E3H2ZE) PHENOXYETHANOL (UNII: HIE492ZZ3T) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) WATER (UNII: 059QF0KO0R) ZINC OXIDE (UNII: SOI2LOH54Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61924-205-04 100 g in 1 TUBE; Type 0: Not a Combination Product 04/18/2011 2 NDC:61924-205-07 198 g in 1 TUBE; Type 0: Not a Combination Product 04/18/2011 3 NDC:61924-205-05 5 g in 1 PACKET; Type 0: Not a Combination Product 04/18/2011 4 NDC:61924-205-15 15 g in 1 PACKET; Type 0: Not a Combination Product 04/18/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 04/18/2011 Labeler - DermaRite Industries, LLC (883925562)