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 INGREDIENT

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)