Durma DynaGel by Dynarex Corporation DURMA DYNAGEL gel

Durma DynaGel by

Drug Labeling and Warnings

Durma DynaGel by is a Otc medication manufactured, distributed, or labeled by Dynarex Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Glycerin 20%

Purpose

Skin Protectant

Use(s)

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

For External Use Only

Do not use on

deep or puncture wounds Animal bites

When using this product

Avoid contact with eyes.

Stop use and ask a doctor if

Condition worsens or does not improve withing 10-14 days

Keep out of reach of children.

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

Directions

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

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

Inactive Ingredients

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?

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

Label

1280 Durma DynaGel

INGREDIENTS AND APPEARANCE

DURMA DYNAGEL 
durma dynagel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67777-236
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	20 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
EDETATE SODIUM (UNII: MP1J8420LU)
METHYLPARABEN (UNII: A2I8C7HI9T)
POLYOXYL 60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALLANTOIN (UNII: 344S277G0Z)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Product Characteristics
Color		Score
Shape	FREEFORM	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67777-236-02	24 in 1 CASE	08/21/2025
1	NDC: 67777-236-01	84.7 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	M016	08/21/2025

Labeler - Dynarex Corporation (008124539)