AQUANIL HC- hydrocortisone lotion 
Person and Covey

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Aquanil HC

Active Ingredient

Hydrocortisone

Stop Use and Ask a Doctor

Stop use and ask a doctor if:

-Condition worsens

-If symptoms persit for more than 7 days or clear up and occur again within a few days. Discocntinue use of this product and do not begin use of any other hydrocortisone product unless you have consulted a doctor.

-Do no use for diaper rash. Consult a doctor.

Keep out of the Reach of Children

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

Purpose

Antipruritic (Anti-itch)

Directions

-Shake will before using.

-For adults and children 2 years of age and older: Apply to affected area not more than 2 to 4 times daily.

-For children under 2 years of age: there is no recommended dosage except under the advice and supervision of a ddoctor.

-Store away from excessive heat or cold.

Inactive Ingredients

Purified Water, Glycerin, Cetyl Alcohol, Benzyl Alcohol, Sodium Laureth Sulfate, Stearyl Alcohol, Simethicone, Xanthan Gum

Questions?

Questions? Please call (800) 423-2341

Uses

For the temporary relief of minor skin irritations, inflamaations, itching and rashes caused by:

-insect bites

-eczema

-psoriasis

-soaps

-detergents

-cosmetics,

-jewelry,

-poison oak,

-poison sumac

-Other uses of this product should be undertaken only under the advice and supervision of a doctor.

Warnings

For external use only.

Do not get into eyes. If contact occurs, rinse thoroughly with water.

Package Label. Principal Display Panel

Aquanil HC

AQUANIL HC 
hydrocortisone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0096-0732
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE0.01 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
BENZYL ALCOHOL (UNII: LKG8494WBH)  
WATER (UNII: 059QF0KO0R)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
XANTHAN GUM (UNII: TTV12P4NEE)  
GLYCERIN (UNII: PDC6A3C0OX)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0096-0732-04118 g in 1 BOTTLE; Type 0: Not a Combination Product01/08/1995
2NDC:0096-0732-1516 g in 1 BOTTLE; Type 0: Not a Combination Product01/08/199501/07/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01501/08/1995
Labeler - Person and Covey (008482473)
Establishment
NameAddressID/FEIBusiness Operations
Person and Covey008482473manufacture(0096-0732)

Revised: 12/2023
Document Id: 0cf91b03-89d7-7bd3-e063-6294a90a7fab
Set id: 6b9258e4-c7c4-765e-e053-2991aa0a9f4e
Version: 7
Effective Time: 20231220
 
Person and Covey