Indications and 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
Wound Gel
- Manufacturer
- Lavior Pharma Inc
- Effective date
- 2024-10-22
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 8
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 20:51:34
Label at a glance#
ProductWound Gel
Active ingredientALLANTOIN
Label structure13 sections
Dosage and administration
apply a thin layer 1 to 2 times daily, or as directed by a doctor
Storage and handling
Store at room temperature
Contacts and useful links#
Websitewww.lavior.com
www.lavior.com
www.lavior.comLabel contents#
Full prescribing information#
Active Ingredient
Allantoin 0.5%................................Skin Protectant
Purpose
Skiin 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, Aloe Barbadensis Leaf Juice, Phenoxyethanol, Propanediol, Tocopheryl Acetate, Ethylhexylglycerin, Sodium Gluconate, Citric Acid, Sodium Hyaluronate, Potassium Sorbate, Sodium Benzoate
Questions?
Call (305) 627-3680 or visit www.lavior.com
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 71521-037-15 | 2026-01-29 | C162847 | 48780-1 | 49896155-c1bb-586f-e063-e6dba90add90 | bdd10ce8-1354-2d9a-e053-2a95a90ad848 |
| 71521-037-50 | 2026-01-29 | C162847 | 48780-1 | 49896155-c1bb-586f-e063-e6dba90add90 | bdd10ce8-1354-2d9a-e053-2a95a90ad848 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Wound Gel
- Allantoin
- ETHYLHEXYLGLYCERIN
- SODIUM GLUCONATE
- CITRIC ACID MONOHYDRATE
- SODIUM BENZOATE
- HYALURONATE SODIUM
- POTASSIUM SORBATE
- XANTHAN GUM
- ALOE VERA LEAF
- PHENOXYETHANOL
- PROPANEDIOL
- .ALPHA.-TOCOPHEROL ACETATE, DL-
- DITTRICHIA VISCOSA WHOLE
- GLYCERIN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 71521-037 | 71521-037-50, 71521-037-15 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 4df3b76f-6164-b245-e063-6394a90aca55 | bdd10ce8-1354-2d9a-e053-2a95a90ad848 | 2026-03-26 | Warnings | bdd10ce8-1354-2d9a-e053-2a95a90ad848 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.