DR H STABILIZER- hydrocortisone lotion 
SV Labs Prescott

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ACTIVE INGREDIENT

HYDROCORTISONE 0.75%

PURPOSE

ANTI-ITCH

USES

PROVIDES HELP TO ITCHING ASSOCIATED WITH MINOR SKIN IRRITATION, ECZEMA, PSORIASIS, AND SEBORRHEIC DERMATITIS. OTHER USES OF THIS PRODUCT SHOULD BE UNDER THE ADVICE AND SUPERVISION OF A DOCTOR.

WARNINGS

DISCONTINUE IF CONDITION IS NOT IMPROVING AND CONSULT YOUR PHYSICIAN.

DIRECTIONS

APPLY THIN LAYER TO AFFECTED AREA TWICE DAILY. DO NOT USE FOR MORE THAN 2 WEEKS WITHOUT PHYSICIAN SUPERVISION.

KEEP OUT OF REACH OF CHILDREN.

INACTIVE INGREDIENTS

WATER, PETROLATUM, GLYCERIN, STEARETH-2, DIMETHICONE, CETYL ALCOHOL, MAGNESIUM ALUMINUM SILICATE, BENZYL ALCOHOL, LAURETH-23, SULFUR, CARBOMER, METHYLPARABEN, PROPYLPARABEN, POTASSIUM SORBATE, XANTHAN GUM, SODIUM HYDROXIDE, FRAGRANCE.

OTHER INFORMATION

CONTAINS THE PURE ELEMENT SULFUR AND IS NOT RELATED TO "SULFA ALLERGY".

DrH Stabilizer Lotion 2 oz. - 60 ml.jpg

DR H STABILIZER 
hydrocortisone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62172-203
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE0.75 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PETROLATUM (UNII: 4T6H12BN9U)  
GLYCERIN (UNII: PDC6A3C0OX)  
STEARETH-2 (UNII: V56DFE46J5)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
LAURETH-23 (UNII: N72LMW566G)  
SULFUR (UNII: 70FD1KFU70)  
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62172-203-2260 mL in 1 TUBE; Type 0: Not a Combination Product05/16/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01705/16/201602/01/2018
Labeler - SV Labs Prescott (185073996)

Revised: 1/2024
 
SV Labs Prescott