DIABETIC WOUND GEL- allantoin gel

Diabetic Wound Gel by

Drug Labeling and Warnings

Diabetic Wound Gel by is a Otc medication manufactured, distributed, or labeled by Lavior Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Allantoin 0.5%.......................Skin Protectant

Purpose

Skin Protectant

Uses

• helps prevent and relieve dry, chafed, chapped, or cracked skin
• temporarily protects minor cuts, scrapes, and burns
• helps protect from the drying effects of wind and cold weather

Warnings

For external use only

When using this product

• avoid contact with eyes

Stop use and ask a doctor if

• condition worsens
• symptoms last more than 7 days, clear up and occur again within a few days

Do not use

• deep or puncture wounds
• animal bites
• serious burns

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

apply a thin layer 1 to 2 times daily, or as directed by a doctor

Other information

store at room temperature

Inactive Ingredients

Water/Aqua/Eau, Glycerin, Inula Viscosa Flower/Leaf/Stem Extract, Xanthan Gum, Phenoxyethanol, Propanediol, Tocopheryl Acetate, Ethylhexylglycerin, Sodium Gluconate, Citric Acid, Sodium Hyaluronate

Questions?

Call toll free 1844-474-2552 or visit www.lavior.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DIABETIC WOUND GEL 
allantoin gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71521-036
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
XANTHAN GUM (UNII: TTV12P4NEE)
PROPANEDIOL (UNII: 5965N8W85T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM GLUCONATE (UNII: R6Q3791S76)
DITTRICHIA VISCOSA WHOLE (UNII: 3SYW69FH88)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71521-036-50	50 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/31/2021
2	NDC: 71521-036-15	15 g in 1 TUBE; Type 0: Not a Combination Product	03/17/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	03/31/2021

Labeler - Lavior Pharma Inc (080685327)