KENKODERM ECZEMA HONEY SOOTHING BODY- kenkoderm eczema honey soothing body lotion chewable gel

Kenkoderm Eczema Honey Soothing Body by

Drug Labeling and Warnings

Kenkoderm Eczema Honey Soothing Body by is a Otc medication manufactured, distributed, or labeled by Guangzhou Ariel Biotech Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

1.0% Colloidal Oatmeal

0.5% Allantoin

Purpose

Skin Protectant

Warnings

For external use only.

Do not use

Do not use on deep or puncture wounds, animal bites, serious burns.

WHEN USING

When using this product, do not get into eyes. Stop use and ask a doctor if

condition worsens
symptoms last more than 7 days or clear up and occur again within a few days

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

Other information

store at room temperature
avoid excessive heat

Inactive ingredients

Water(Aqua), Aloe Barbadensis Leaf Water, Caprylic/Capric Triglyceride,
Glycerin, Cetearyl Alcohol, Butyrospermum Parkii (Shea Butter),
Ethylhexyl Palmitate, Squalane, Trehalose, Cetearyl Olivate, Sorbitan
Olivate, Persea Gratissima (Avocado) Oil, Mel (Honey), 1,2-Hexanediol,
Hydroxyacetophenone, Glyceryl Stearate, PEG-100 Stearate, Carbomer, Arginine,
Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer,
Sodium Hyaluronate.

Use

temporarily protects and helps relieve
minor skin irritation and itching due to
eczema, psoriasis, rashes, or dry skin.
helps restore and maintain the skin’s
natural moisture barrier.

Directions

apply to affected area as needed
suitable for daily use
for best results, apply after bathing while skin is still damp

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

KENKODERM ECZEMA HONEY SOOTHING BODY 
kenkoderm eczema honey soothing body lotion chewable gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84148-019
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.5 g  in 100 mL
OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y)	OATMEAL	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ARGININE (UNII: 94ZLA3W45F)
PEG-100 STEARATE (UNII: YD01N1999R)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF OIL (UNII: JQ7YW886UQ)
GLYCERIN (UNII: PDC6A3C0OX)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
SQUALANE (UNII: GW89575KF9)
TREHALOSE (UNII: B8WCK70T7I)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
SORBITAN OLIVATE (UNII: MDL271E3GR)
PERSEA GRATISSIMA (AVOCADO) OIL (UNII: 6VNO72PFC1)
MEL (UNII: Y9H1V576FH)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
CARBOMER (UNII: 0A5MM307FC)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84148-019-01	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/15/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	01/15/2026

Labeler - Guangzhou Ariel Biotech Co., Ltd. (402818771)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Ariel Biotech Co., Ltd.		402818771	manufacture(84148-019)