ANTI-ITCH VULVA CREAM 1 HYDROCORTISONE ACETATE- hydrocortisone acetate cream 
The Honey Pot Company LLC

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Anti-Itch Vulva Cream 1 % Hydrocortisone Acetate

Drug Facts

Active Ingredient

Hydrocortisone Acetate 1%

Purpose

Anti-Itch

Uses:

For the temporary relief of external feminine itching.

Warnings:

For external use only

When using this product:

avoid contact with eyes.

Stop use and ask doctor if:

  • Condition worsens
  • If symptoms persist for more than 7 days, or clear up and reoccur again within a few days

Do not use if:

you have vaginal discharge. Consult a physician.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away

Directions:

Apply to affected area not more than 3 to 4 times daily. Adults and children 12 years of age and older:Children under 12 years of age: Consult a doctor

Inactive Ingredients:

Adansonia Digitata Seed Oil, Allantoin, Aloe Barbadensis Leaf Juice, Butyrospermum Parkii (Shea) Butter, C10-18 Triglycerides, Candelilla/Jojoba/Rice Bran Polyglyceryl-3 Esters, Caprylhydroxamic Acid, Caprylyl Glyceryl Ether, Ceramide NG, Cetearyl Alcohol, Cetyl Alcohol, Cholesterol, Citric Acid, Cocos Nucifera (Coconut) Oil, Ethoxydiglycol, Glyceryl Stearate, Helianthus Annuus (Sunflower) Seed Oil, Helianthus Annuus (Sunflower) Seed Wax, Hydroxyethylcellulose, Lavandula Angustifolia (Lavender) Oil, Limonene, Linalool, Melia Azadirachta Seed Oil, Mentha Piperita (Peppermint) Oil, Myristyl Alcohol, Polyhydroxystearic Acid, Potassium Sorbate, Propanediol, Propolis Extract, Simmondsia Chinensis (Jojoba) Seed Oil, Sodium Benzoate, Sodium Phytate, Sodium Stearoyl Lactylate, Steareth-30, Stearic Acid, Steary Alcohol, Sucrose Palmitate, Theobroma Cacao (Cocoa) Seed Butter, Water, Xanthan Gum

Questions:

For questions and general information visit us at www.thehoneypot.co/contact

Package Labeling:

Label

inner_labek

ANTI-ITCH VULVA CREAM 1 HYDROCORTISONE ACETATE 
hydrocortisone acetate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82637-9455
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROCORTISONE ACETATE (UNII: 3X7931PO74) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE ACETATE10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
LAVENDER OIL (UNII: ZBP1YXW0H8)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
LINALOOL, (+/-)- (UNII: D81QY6I88E)  
AZADIRACHTA INDICA SEED OIL (UNII: 4DKJ9B3K2T)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
MYRISTYL ALCOHOL (UNII: V42034O9PU)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PROPANEDIOL (UNII: 5965N8W85T)  
PROPOLIS WAX (UNII: 6Y8XYV2NOF)  
JOJOBA OIL (UNII: 724GKU717M)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
PHYTATE SODIUM (UNII: 88496G1ERL)  
SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)  
STEARETH-30 (UNII: 5776GCL1DG)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
SUCROSE PALMITATE (UNII: 3OSQ643ZK5)  
COCOA BUTTER (UNII: 512OYT1CRR)  
WATER (UNII: 059QF0KO0R)  
XANTHAN GUM (UNII: TTV12P4NEE)  
ADANSONIA DIGITATA SEED OIL (UNII: 77MKL7AR5I)  
ALLANTOIN (UNII: 344S277G0Z)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
SHEA BUTTER (UNII: K49155WL9Y)  
C10-18 TRIGLYCERIDES (UNII: 43AGM4PHPI)  
CANDELILLA WAX (UNII: WL0328HX19)  
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
CAPRYLYL GLYCERYL ETHER (UNII: MI97BW74XZ)  
CERAMIDE NG (UNII: C04977SRJ5)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
CHOLESTEROL (UNII: 97C5T2UQ7J)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
COCONUT OIL (UNII: Q9L0O73W7L)  
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
SUNFLOWER OIL (UNII: 3W1JG795YI)  
HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82637-9455-11 in 1 CARTON03/01/2022
130 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01703/01/2022
Labeler - The Honey Pot Company LLC (045600502)

Revised: 10/2023
Document Id: 08157e2c-2c75-1487-e063-6394a90a1092
Set id: 6f32b536-6ebf-49a8-abb6-2a1daae2f6d7
Version: 2
Effective Time: 20231019
 
The Honey Pot Company LLC