CVS MAXIMUM STRENGTH ANTI-ITCH CREAM- hydrocortisone 1% cream

CVS Maximum Strength Anti-Itch Cream by

Drug Labeling and Warnings

CVS Maximum Strength Anti-Itch Cream by is a Otc medication manufactured, distributed, or labeled by CVS Health, Medical Products Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Hydrocortisone 1.0%

PURPOSE

Anti-itch

INDICATIONS & USAGE

Temporarily relieves external feminine itching

WARNINGS

Avoid contact with the eyes

If you are allergic to any of the ingredients

Stop use and ask the doctor if :

• conditions worsen
• symptoms last ore than 7 days, or clear up and occur again within a few days

If swallowed, get medical help or contact a poison control center right away.

DOSAGE & ADMINISTRATION

• Adults and children 12 years and over: Apply to the external vaginal area more than 3 times a day
• Children under 12 years: Consult a doctor

OTHER SAFETY INFORMATION

Store at 20-25 C (68-77 F)

INACTIVE INGREDIENT

aloe vera, Ascorbic acid, Cetyl alcohol, Citric acid, Glyceryl stearate, Mineral oil, PEG-100 Stearate, PEG-150 Distearate, Petrolatum, Phenoxyethanol, Polycarbophil, Propylene Glycol, Purified Water, Sodium citrate, Stearyl alcohol, Vitamin A palmitate, Vitamin E acetate, Xanthan Gum.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CVS MAXIMUM STRENGTH ANTI-ITCH CREAM 
hydrocortisone 1% cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-485
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
POLYCARBOPHIL (UNII: W25LM17A4W)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
MINERAL OIL (UNII: T5L8T28FGP)
CETYL ALCOHOL (UNII: 936JST6JCN)
WATER (UNII: 059QF0KO0R)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
XANTHAN GUM (UNII: TTV12P4NEE)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
PETROLATUM (UNII: 4T6H12BN9U)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-485-08	113 g in 1 TUBE; Type 0: Not a Combination Product	04/06/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	04/06/2022

Labeler - CVS Health (062312574)

Registrant - Medical Products Laboratories, Inc. (008965063)