DERMFREE ANTI-ITCH- hydrocortisone1% anti-itch cream

DERMFREE Anti-itch by

Drug Labeling and Warnings

DERMFREE Anti-itch by is a Otc medication manufactured, distributed, or labeled by Jiangxi Yudexi Pharmaceutical Co., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Hydrocortisone 1%

Purpose

Anti-itch

Use

temporarily relieves pain and itching associated with:▇insect bites▇ minor burns ▇sunburn▇ minor skin irritations▇ minor cuts ▇scrapes▇ rashes due to poison ivy, poison oak, and poison sumac ▇dries the oozing and weeping of poison ivy, poison oak ，and poison sumac

Warnings

For external use only.

Do not use

▇on large areas of the body ▇with any other product containing diphenhydramine, even one taken bymouth

When Using

avoid contact with eyes

Stop Use

▇condition worsens or does not improve within 15 days ▇symptoms persist for more than 15 days or clear up and occur again within a few days

Ask Doctor

▇on chicken pox ▇ on measles

Keep Oot Of Reach Of Children

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

Directions

▇do not use more than directed ▇adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily ▇children under 2 years of age: Consult a doctor before use.

Other information

▇protect from excessive heat (40°C/104°F)

Inactive ingredients

water,Glycerol,Propylene Glycol,Polydimethylsiloxane,Trolamine.Borneol,MENTHA PIPERITA, Methylparaben, Chlorhexidine

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DERMFREE ANTI-ITCH 
hydrocortisone1% anti-itch cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85248-126
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
DIMETHICONE (UNII: 92RU3N3Y1O)
BORNEOL (UNII: M89NIB437X)
METHYLPARABEN (UNII: A2I8C7HI9T)
CHLORHEXIDINE (UNII: R4KO0DY52L)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
MENTHA PIPERITA (UNII: 79M2M2UDA9)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85248-126-01	42.5 g in 1 BOTTLE; Type 0: Not a Combination Product	02/09/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	02/09/2026

Labeler - Jiangxi Yudexi Pharmaceutical Co., LTD (455662836)