HYDROCORTISONE PLUS 12 MOISTURIZERS- hydrocortisone cream 
RITE AID CORPORATION

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Hydrocortisone Plus 12 Moisturizers

Drug Facts

Active ingredient

Hydrocortisone 1%

Purpose

Anti-itch

Uses

Warnings

For external use only

Do not use

  • in the genital area if you have a vaginal discharge. Consult a doctor.
  • for the treatment of diaper rash. Consult a doctor.

When using this product

  • avoid contact with eyes
  • do not use more than directed unless told to do so by a doctor
  • do not put directly into the rectum by using fingers or any mechanical device or applicator

Stop use and ask a doctor if

  • condition worsens, symptoms persist for more than 7 days or clear up and occur again within a few days, and do not begin use of any other hydrocortisone product unless you have asked a doctor
  • rectal bleeding occurs

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

aloe powder, cetearyl alcohol/sodium lauryl sulfate/sodium cetearyl sulfate, chamomile oil, citric acid, corn oil, glycerin, glyceryl monostearate, isopropyl palmitate, maltodextrin, methylparaben, mineral oil, paraffin wax, propylene glycol, propylparaben, purified water, stearyl alcohol, vitamin A & vitamin D3 liquid, vitamin E, white petrolatum.

Questions?

Call 1-866-923-4914

DISTRIBUTED BY:
RITE AID, 200 NEWBERRY COMMONS ETTERS, PA 17319
www.riteaid.com

MADE IN CANADA

PRINCIPAL DISPLAY PANEL - 56.8 Tube Carton

MAXIMUM STRENGTH

HYDROCORTISONE CREAM 1%

PLUS 12 MOISTURIZERS

ANTI-ITCH

RELIEVES ITCH FAST

For skin irritations

• Enriched with vitamins A, D3 & Vitamin E

NET WT 1 OZ (28.4 hydrocortisone-01 g)

HYDROCORTISONE  PLUS 12 MOISTURIZERS
hydrocortisone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-2090
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)  
CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
CORN OIL (UNII: 8470G57WFM)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
MINERAL OIL (UNII: T5L8T28FGP)  
PARAFFIN (UNII: I9O0E3H2ZE)  
PETROLATUM (UNII: 4T6H12BN9U)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
CHOLECALCIFEROL (UNII: 1C6V77QF41)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11822-2090-21 in 1 CARTON07/21/2023
128.4 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:11822-2090-31 in 1 CARTON07/21/2023
256.8 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01707/21/2023
Labeler - RITE AID CORPORATION (014578892)
Registrant - TARO PHARMACEUTICALS U.S.A., INC. (145186370)
Establishment
NameAddressID/FEIBusiness Operations
Taro Pharmaceuticals Inc.206263295manufacture(11822-2090)

Revised: 4/2024
Document Id: 162892da-5d4c-86c6-e063-6394a90abdff
Set id: 05598255-3e7a-46a5-ae7e-dcfcb616d59d
Version: 3
Effective Time: 20240415
 
RITE AID CORPORATION