FDA.reportPublic FDA data

Nasal Dryness Relief Gel

Manufacturer
Genuine Virgin Aloe Corporation
Effective date
2026-01-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:35:16

Label at a glance#

ProductNasal Dryness Relief Gel
Active ingredientALLANTOIN
Label structure14 sections

Indications and uses

Temporarily protects and helps relieve chapped or cracked skin Helps protect from the drying effects of wind and cold weather

Dosage and administration

Apply a thin layer to external nasal passages area(s) as often as needed. May also be used on other facial areas to help relieve disconfort. For CPAP mask users: Before each use, apply a thin layer to nasal area and wherever mask touches the skin. After each use, apply gel to mask lines to replenish moisture and revitalize skin.

Storage and handling

Store at room temperature

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Allantoin 0.5%

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Uses

INSTRUCTIONS FOR USE SECTION

  • Temporarily protects and helps relieve chapped or cracked skin
  • Helps protect from the drying effects of wind and cold weather

Warnings

WARNINGS SECTION

For external use only.

Don not use

OTC - DO NOT USE SECTION

  • on deep puncture wounds
  • on infection
  • on lacerations

When using this product

OTC - WHEN USING SECTION

do not get into eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens or does not improve within 7 days.

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,.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply a thin layer to external nasal passages area(s) as often as needed. May also be used on other facial areas to help relieve disconfort.

For CPAP mask users: Before each use, apply a thin layer to nasal area and wherever mask touches the skin. After each use, apply gel to mask lines to replenish moisture and revitalize skin.

Other information

STORAGE AND HANDLING SECTION

  • Store at room temperature

Questions?

OTC - QUESTIONS SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

water, aloe barbadensis (aloe vera) leaf juice*, carbomer, arginine, ethylhexylglycerin, phenoxyethanol.

*Certified Organic Ingredient - Mayacert Certifier

Indications & Usage Section

Temporarily protects and helps relieve chapped or cracked skin * Helps protect from the drying effects of wind and cold weather

Labels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Nasal Dryness ReliefNasal Dryness ReliefNasal Dryness Relief_1oz_label

Nasal Dryness ReliefNasal Dryness Relief

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10738-051-102026-01-27C16284748780-11030e365-43d2-111a-e063-dadaa90a10e2TriDerma Nasal Dryness Relief Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10738-051-10Nasal Dryness Relief Gel1 in 1 CARTONGEL12
10738-051-15Nasal Dryness Relief Gel28 g in 1 TUBEGEL282

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10738-05110738-051-15, 10738-051-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
ARGININE94ZLA3W45FIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PHENOXYETHANOLHIE492ZZ3TIACT
CARBOMER 934Z135WT9208IACT
ALLANTOIN344S277G0ZACTIB
WATER059QF0KO0RIACT

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
Nasal Dryness Relief GelALLANTOINGenuine Virgin Aloe Corporationdfece059-57bd-8eee-e053-2a95a90a980e2026-01-27WarningsExact identifier
ndc (package): 10738-051-15
ndc (package): 10738-051-10
ndc (product): 10738-051
ndc11 (package): 10738005115
ndc11 (package): 10738005110
spl id: 49655e27-0a67-4fca-e063-6294a90a5cfa
spl set id: dfece059-57bd-8eee-e053-2a95a90a980e

Reported adverse events (FAERS/openFDA)#

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