LuraDRox Rx Wound Gel
- Manufacturer
- Alvix Laboratories
- Effective date
- 2019-03-27
- Label type
- PRESCRIPTION MEDICAL DEVICE LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 00:28:45
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
DESCRIPTION
LuraDroxᵀᴹ Rx Wound Gel is a wound dressing hydrogel that helps maintain a moist wound environment that is conducive to healing by either absorbing or donating moisture and wound exudates.
INDICATIONS FOR USE
LuraDroxᵀᴹ Rx Wound Gel is indicated for use in the management of 1st and 2nd degree burns, wounds such as stasis ulcers, pressure ulcers, diabetic ulcers, lacerations, abrasions, skin tears, surgical incision sites, device insertion site wounds, graft sites and donor sites.
PRECAUTIONS
1. Always use LuraDroxᵀᴹ Rx Wound Gel exactly as indicated by the prescribing physician. Consult with a healthcare professional if you have any concerns or questions about the wound.
2. Always be alert for signs of wound infection or worsening conditions. These can include:
- Pus or cloudy fluid draining from the wound
- Increased redness around the wound
- Wound has become extremely tender
- Increased pain or swelling 48 hours after the wound occurred
- Onset of fever
3. The gel is designed for use on any part of the body except for oral and ophthalmic use. Do not use the gel in any other manner.
HOW TO APPLY
Home use of LuraDroxᵀᴹ Rx Wound Gel should only be allowed if indicated by the prescribing physician. Always use LuraDroxᵀᴹ Rx Wound Gel exactly as indicated by the prescribing physician.
1. Wash your hands with soap and water before touching the wound.
2. Carefully clean the wound using soap and water, or as otherwise directed by the prescribing physician.
3. Dispense gel onto an appropriate clean applicator (such as a tongue depressor or gauze) in a sufficient amount to liberally cover the wound. Cover the gel if desired with a secondary cover such as a gauze dressing wrap, film or non-woven adhesive secondary dressing.
4. Remove product from the skin within 24 hours by cleaning the wound site with soap and water.
5. Discard remaining product.
INGREDIENTS
Deionized water, carbopol, silver as nanoparticles, sodium hyaluronate (0.1%), sodium hydroxide
HOW SUPPLIED
LuraDroxᵀᴹ Rx Wound Gel is supplied in a 5 ML squeezable sachet. 15455-9569-01
PRESCRIPTION MEDICAL DEVICE:FEDERAL LAW RESTRICTS THIS DEVICE TO SALE BY OR ON THE ORDER OF A PHYSICIAN
STORE AT ROOM TEMPERATURE
Keep this and other similar products out of the reach of children.
Alvix Laboratories, LLC
6601 Sunplex Drive
Ocean Springs, MS 39564
1 888 526 5449
LuraDrox Rx Wound Gel Package Insert
LuraDrox Rx Wound Gel Primary Label
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 15455-9569-1 | ML - Milliliter | 15455-9569 | 3613f2f7-c2e1-45dc-a36d-d9c4ff8968ba | 1 | 2019-04-11 |
Products#
Every source-derived product name is available through these pages.
- LuraDRox Rx Wound Gel
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 15455-9569 | 15455-9569-1 |
Source Document#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

