DERMELEVE- aluminum acetate cream 
Advanced Derm Solutions LLC

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Active Ingredient

Aluminum acetate (0.2%)

Purpose

Astringent

Uses

• Insects Bites
• Minor Burn
• Athlete's foot 
• Poison lvy 
• Poison oak
• Poison sumac 
• Rashes cause by soaps, detergents, cosmetic or jewelry

Warnings

For external use only.
Avoidcontact with eyes.
Do not applyto open wounds.
STOP USEand ask a physician if condition worsens
or symptoms persist for more than seven days.

■ Keep out of reach of children.

Directions

Adults and children two years of age and older,
apply to affected area as needed or as directed by a physician. Consult a physician for children under the age of two.

Inactive ingredients 

Caprylyc/Capric Triglyceride, Caprylyl Glycol, Ceramide NG, Cetearyl Alcohol, Dimethicone 100,
Disodium Edta, Emulsifying Wax NF, Glycerin, Glyceryl Stearate SE, Sodium Hyaluronate, Isopropyl Myristate Magnesium Aluminum Silicate Type IA, Phenoxyethanol, Polyacrylate Crosspolymer-6, Shea Butter, Strontium Nitrate, Tetrahexyldecyl Ascorbate, Tocopherol, Water O-18, Xanthan Gum

Questions ?  Visit  www.dermeleve.com

Manufactured for Advanced Derm Solutions LLC
Oldsmar, FL 34677 | dermeleve.com
U.S. Patents: 5,716,625; 5,804,203; 6,139,850; 7,404,967

Product label

image descriptionimage descriptionimage descriptionimage descriptionimage description

DERMELEVE 
aluminum acetate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81507-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM ACETATE (UNII: 80EHD8I43D) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM ACETATE0.2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CERAMIDE NG (UNII: C04977SRJ5)  
DIMETHICONE 100 (UNII: RO266O364U)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
MAGNESIUM ALUMINUM SILICATE TYPE IA (UNII: SUS08ZOA9S)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
SHEA BUTTER (UNII: K49155WL9Y)  
STRONTIUM NITRATE (UNII: BDG873AQZL)  
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)  
TOCOPHEROL (UNII: R0ZB2556P8)  
WATER O-18 (UNII: 7QV8F8BYNJ)  
XANTHAN GUM (UNII: TTV12P4NEE)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
POLAWAX POLYSORBATE (UNII: Q504PL8E0V)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81507-003-01120 g in 1 TUBE; Type 0: Not a Combination Product02/04/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01602/04/2022
Labeler - Advanced Derm Solutions LLC (117840544)

Revised: 12/2023
Document Id: 0c645754-26ae-f4eb-e063-6294a90a6ed2
Set id: 5dd4c952-8880-4c06-9c09-20c6a3cdd0f5
Version: 4
Effective Time: 20231213
 
Advanced Derm Solutions LLC