Label: PEVIDERM PRAMOXINE HYDROCHOLRIDE 1%- pramoxine hydrochloride lotion
- NDC Code(s): 58980-913-80
- Packager: Stratus Pharmaceuticals Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 7, 2024
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- SPL UNCLASSIFIED SECTION
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 222 mL Bottle Box
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INGREDIENTS AND APPEARANCE
PEVIDERM PRAMOXINE HYDROCHOLRIDE 1%
pramoxine hydrochloride lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58980-913 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Pramoxine Hydrochloride (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) Pramoxine Hydrochloride 1 mg in 1 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glyceryl Stearate/PEG-100 Stearate (UNII: RD25J5V947) PEG-8 Stearate (UNII: 2P9L47VI5E) Calcium Chloride (UNII: M4I0D6VV5M) CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E) Cetyl Palmitate (UNII: 5ZA2S6B08X) Isopropyl Myristate (UNII: 0RE8K4LNJS) White Petrolatum (UNII: B6E5W8RQJ4) Stearic Acid (UNII: 4ELV7Z65AP) Benzyl Alcohol (UNII: LKG8494WBH) Sodium Hydroxide (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58980-913-80 1 in 1 BOX 11/01/2024 1 222 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph drug M017 11/01/2024 Labeler - Stratus Pharmaceuticals Inc (789001641) Establishment Name Address ID/FEI Business Operations Tarmac Products Inc 059890491 MANUFACTURE(58980-913)