TRIDERMA FOOT DEFENSE- triderma foot defense cream cream

TriDerma Foot Defense by

Drug Labeling and Warnings

TriDerma Foot Defense by is a Otc medication manufactured, distributed, or labeled by Genuine Virgin Aloe Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Allantoin 1.5%

PURPOSE

Skin Protectant

INDICATIONS & USAGE

Helps prevent and temporarily protects and helps relieve chafed, chapped or cracked skin.

WARNINGS

For external use only.

DO NOT USE

• on deep puncture wounds
• on infections
• on lacerations

WHEN USING

do not get into eyes

STOP USE

stop use and ask a doctor if conditin worsens or does not improve within 7 days.

KEEP OUT OF REACH OF CHILDREN

if swallowed get medical help and contact a poison control center right away.

DOSAGE & ADMINISTRATION

Apply twice a day or as often as needed.

STORAGE AND HANDLING

• Do not use if the tube seal is broken
• Store at room temperatue

QUESTIONS

Questions: 1-800-279-7282 M-F 8 am - 4 pm PST

INACTIVE INGREDIENT

Aloe Barbadensis (Aloe Vera) Leaf Juice*, Avena Sativa (Oat) Kernel Flour, Butyrospermum Parkii (Shea) Butter, Cera Alba (Beeswax), Cetearyl Alcohol, Cetyl Alcohol, Dimethicone, Ethylhexylglycerin, Isopropyl Palmitate, Lactic Acid, Panthenol (Pro-Vitamin B5), Phenoxyethanol, Polysorbate 60, Sodium Hyaluronate, Sodium Hydroxide, Sodium PCA, Sodium Phytate, Tocopheryl Acetate (Vitamin E), Urea, Water, Zinc PCA.

*Certified Organic Ingredient - Mayacert Certifier

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TRIDERMA FOOT DEFENSE 
triderma foot defense cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10738-064
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	15 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
PANTHENOL (UNII: WV9CM0O67Z)
SODIUM PHYTATE (UNII: 88496G1ERL)
CETYL ALCOHOL (UNII: 936JST6JCN)
SHEA BUTTER (UNII: K49155WL9Y)
LACTIC ACID (UNII: 33X04XA5AT)
BEESWAX (UNII: 2ZA36H0S2V)
SODIUM PCA (UNII: 469OTG57A2)
ZINC PCA (UNII: C32PQ86DH4)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
DIMETHICONE 100 (UNII: RO266O364U)
POLYSORBATE 60 (UNII: CAL22UVI4M)
AVENA SATIVA (OAT) STARCH (UNII: 904CE6697V)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10738-064-40	1 in 1 CARTON	05/31/2025
1	NDC: 10738-064-45	119 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)	05/31/2025

Labeler - Genuine Virgin Aloe Corporation (961374147)

Establishment
Name	Address	ID/FEI	Business Operations
Genuine Virgin Aloe Corporation		961374147	manufacture(10738-064)