Durma DynaGel

Manufacturer
Dynarex Corporation
Effective date
2025-08-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:11:12

Label at a glance#

ProductDurma DynaGel
Active ingredientGLYCERIN
Label structure9 sections

Dosage and administration

• Apply liberally as often as necessary to cover affected areas. • If gauze is used, as a wound covering, moisten first. • Children under 6 months: Consult a doctor before use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Glycerin 20%

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Use(s)

INDICATIONS & USAGE SECTION

• Temporarily protects and helps relieve minor skin irritation and itching of minor cute, scrapes, and burns

• Maintains a moist wound environment

• Ideal for management of stasis ulcers, pressure ulcers (stage 1-4), first second-degree burns, cuts, post-operative incicions, and skin conditions associated with peristomal care

Warnings

WARNINGS SECTION

For External Use Only

Do not use on

OTC - DO NOT USE SECTION

• deep or puncture wounds • Animal bites

When using this product

OTC - WHEN USING SECTION

• Avoid contact with eyes.

Stop use and ask a doctor if

OTC - STOP USE SECTION

• Condition worsens or does not improve withing 10-14 days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply liberally as often as necessary to cover affected areas.

• If gauze is used, as a wound covering, moisten first.

• Children under 6 months: Consult a doctor before use.

Other Information

OTHER SAFETY INFORMATION

• Store at room temperature 15° - 30ºC (59° - 86°F) • Tamper evident. Do not use if seal is damaged.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Allantoin, Aloe Vera Gel, Diazolidinyl Urea, Methylparaben, PEG-4 Olivate, PEG-60 Hydrogenated Castor Oil, Propylene Glycol, Propylparaben, Purified Water, Sodium Polyacrylate, Tetrasodium EDTA, Tocopherol Acetate

Questions?

OTC - QUESTIONS SECTION

• 1-888-DYNAREX Monday - Friday, 9AM - 5PM EST.

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1280_IN_MASTER1280_IN_MASTER1280 Durma DynaGel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2637866glycerin 20 % Topical GelPSN1
2637866glycerin 0.2 MG/MG Topical GelSCD1
2637866glycerin 20 % Topical GelSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
GLYCERIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67777-236-01Durma DynaGel84.7 g in 1 TUBEGEL84.71
67777-236-02Durma DynaGel24 in 1 CASEGEL241

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67777-23667777-236-01, 67777-236-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

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
Durma DynaGelDURMA DYNAGELDynarex Corporation3bcbe314-98ca-78f1-e063-6394a90a13ad2025-08-07WarningsExact identifier
ndc (package): 67777-236-01
ndc (package): 67777-236-02
ndc (product): 67777-236
ndc11 (package): 67777023601
ndc11 (package): 67777023602
spl id: 3bcbe314-98cb-78f1-e063-6394a90a13ad
spl set id: 3bcbe314-98ca-78f1-e063-6394a90a13ad

Reported adverse events (FAERS/openFDA)#

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