Label: DIABETIC WOUND GEL- allantoin gel
- NDC Code(s): 71521-036-15, 71521-036-50
- Packager: Lavior Pharma Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 19, 2023
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- Active Ingredients
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- Do not use
- Keep out of reach of children
- Directions
- Other information
- Inactive Ingredients
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DIABETIC WOUND GEL
allantoin gelProduct 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)