FDA.reportPublic FDA data

TriDerma Aloe Zinc Occlusive

Manufacturer
Genuine Virgin Aloe Corporation
Effective date
2026-01-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:35:59

Label at a glance#

ProductTriDerma Aloe Zinc Occlusive
Active ingredientALLANTOIN
Label structure11 sections

Indications and uses

temporarily protects and helps relieved chafed, chapped or cracked skin.

Dosage and administration

Apply as soon as possible after procedure.  Reapply as often as needed.

Label contents#

Full prescribing information#

PURPOSE

OTC - PURPOSE SECTION

Skin Protectant

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Apply as soon as possible after procedure.  Reapply as often as needed.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice*,
Avena Sativa (Oat) Kernel Flour, Cera Alba (Beeswax),
Butyrospermum Parkii (Shea) Butter, Cetearyl Alcohol, Cetyl
Alcohol, Dimethicone, Ethylhexylglycerin, Glyceryl Stearate,
Glyceryl Stearate SE, Helianthus Annuus (Sunflower) Seed
Oil, Isopropyl Palmitate, Panthenol (Pro-Vitamin B5),
Phenoxyethanol, Polysorbate 60, Potassium Cetyl
Phosphate, Propanediol, Sodium Hyaluronate, Sodium
Hydroxide, Sodium PCA, Sodium Phytate, Tocopheryl
Acetate (Vitamin E), Water (Aqua), Xanthan Gum, Zinc PCA.

*Certified Organic Ingredient - Mayacert Certifier

WARNINGS

WARNINGS SECTION

For external use only

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Allantoin 1.5%

USES

INDICATIONS & USAGE SECTION

temporarily protects and helps relieved chafed, chapped or cracked skin.

DO NOT USE:

OTC - DO NOT USE SECTION

on deep puncture wounds, on infections, on lacerations

WHEN USING THIS PRODUCT:

OTC - WHEN USING SECTION

do not get into eyes

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

STOP USE AND ASK A DOCTOR IF:

OTC - STOP USE SECTION

condition worsens or does not improve within 7 days.

PACKAGING

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

post 2 oz label.jpgpost 2 oz label.jpgpost 3.3 label.jpgpost 3.3 label.jpg

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130182228000335GTIN-13: 0182228000335
EAN-13: 0182228000335
GTIN-12: 182228000335
UPC-A: 182228000335
GTIN storage (14 digits): 00182228000335		post 3.3 label.jpg, post 2 oz label.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10738-123-25TriDerma Aloe Zinc Occlusive57 g in 1 TUBECREAM571
10738-123-35TriDerma Aloe Zinc Occlusive94 g in 1 TUBECREAM941

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10738-12310738-123-35, 10738-123-25

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHICONE 100RO266O364UIACT
BEESWAX2ZA36H0S2VIACT
ALOE VERA LEAF JUICERUE8E6T4NBIACT
SHEA BUTTERK49155WL9YIACT
ALLANTOIN344S277G0ZACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
TriDerma Aloe Zinc OcclusiveBARRIERGenuine Virgin Aloe Corporationa8c858b7-8ce5-40ef-a5f6-e60a9420721d2026-01-30WarningsExact identifier
ndc (package): 10738-123-35
ndc (package): 10738-123-25
ndc (product): 10738-123
ndc11 (package): 10738012335
ndc11 (package): 10738012325
spl id: 49a27d36-cf62-9a89-e063-6394a90a92c6
spl set id: a8c858b7-8ce5-40ef-a5f6-e60a9420721d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.