DYNAREX HYDROGEL- glycerin gel

Dynarex Hydrogel by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient

Active Ingredient                  Purpose

Glycerin 20.0%                    Skin Protectant

Purpose

For dressing and management of stasis ulcers, pressure ulcers (stages I-IV) 1st and 2nd degree burns, cuts abrasions, skin irritations, post operative incisions, and skin conditions associated with peristomal care.

Warnings

• If condition worsens or does not improve within 10-14 days, consult a physician.
• Keep this and all medications out of the reach of children.
• Follow directions for use.
  

Dosage & Administration Dynarex Hydrogel

• Apply Wound Gel liberally to cover involved areas; apply as often as necessary.
• If gauze is used as a wound covering, moisten first.
  

Keep out of reach of children

• KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN

Indications and Usage:

Use:

• For dressing and management of stasis ulcers,
  
• pressure ulcers (stages I-IV)
  
• 1st and 2nd degree burns,
  
• cuts abrasions,
  
• skin irritations,
  
• post operative incisions,
  
• and skin conditions associated with peristomal care.

Inactive Ingredient

Inactive ingredients: Allantoin, aloe barbadensis gel, diazolidinyl urea, methyparaben, PEG-4 Olivate, PEG-60 hydrogenated castor oil, propylene glycol, propylparaben, purified water, sodium polyacrylate, tetrasodium EDTA, tocopherol acetate.

Principal Display

Principal Display

Dynarex_Hydrogel.jpg

INGREDIENTS AND APPEARANCE

DYNAREX HYDROGEL 
glycerin gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67777-233
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
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYOXYL 60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
EDETATE SODIUM (UNII: MP1J8420LU)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALLANTOIN (UNII: 344S277G0Z)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67777-233-01	84.7 g in 1 TUBE; Type 0: Not a Combination Product	05/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part346	05/26/2010

Labeler - Dynarex Corporation (008124539)

Registrant - Dynarex Corporation (008124539)