TRIDERMA STUBBORN ECZEMA ITCH RELIEF- stubborn e relief cream

TriDerma Stubborn Eczema Itch Relief by

Drug Labeling and Warnings

TriDerma Stubborn Eczema Itch Relief by is a Otc medication manufactured, distributed, or labeled by Genuine Virgin Aloe Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WARNINGS

For external use only

PURPOSE

Skin Protectant

DIRECTIONS

apply twice a day or as often as needed.

INACTIVE INGREDIENTS

Allantoin, Aloe Barbadensis Leaf Juice*, Arnica Montana Flower Extract, Avena Sativa Kernel Oil, Butyrospermum Parkii (Shea) Butter, Cera Alba (Beeswax), Cetearyl Alcohol, Cetyl Alcohol, Dimethicone, Ethylhexylglycerin, Glycerin, Isopropyl Palmitate, Lactic Acid, Panthenol (Pro-Vitamin B5), Phenoxyethanol, Polysorbate 60, Sodium Hyaluronate, Sodium PCA, Sodium Phytate, Tocopheryl Acetate (Vitamin E), Urea, Water, Zinc PCA

*Certified Organic Ingredient - Mayacert Certifier

ACTIVE INGREDIENT

Colloidal Oatmeal 2%

USES

temporarily protects and helps relieve minor skin irritation and itching due to: eczema rashes

DO NOT USE:

on deep puncture wounds, on infections, on lacerations

WHEN USING THIS PRODUCT:

do not get into eyes

KEEP OUT OF REACH OF CHILDREN

if swallowed get medical help and contact a Poison Control Center right away.

STOP USE AND ASK A DOCTOR IF:

condition worsens or does not improve within 7 days.

PACKAGING

INGREDIENTS AND APPEARANCE

TRIDERMA STUBBORN ECZEMA ITCH RELIEF 
stubborn e relief cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10738-169
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y)	OATMEAL	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
DIMETHICONE 100 (UNII: RO266O364U)
BEESWAX (UNII: 2ZA36H0S2V)
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
SHEA BUTTER (UNII: K49155WL9Y)
ALLANTOIN (UNII: 344S277G0Z)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
AVENA SATIVA (OAT) KERNEL OIL (UNII: 3UVP41R77R)
PANTHENOL (UNII: WV9CM0O67Z)
CETYL ALCOHOL (UNII: 936JST6JCN)
SODIUM PCA (UNII: 469OTG57A2)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10738-169-40	1 in 1 PACKAGE	01/30/2028
1	NDC: 10738-169-45	113 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/30/2026

Labeler - Genuine Virgin Aloe Corporation (961374147)

Establishment
Name	Address	ID/FEI	Business Operations
Genuine Virgin Aloe Corporation		961374147	manufacture(10738-169)