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Renuu NL Patch

Generic Name: allantoin, petrolatum
Dosage Form: patch

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

RENUU NL

Other Ingredients vitamin E, Lidocaine, onion extract

Active Ingredient

Allantoin 2.00 %

Petrolatum 30.00 %

Purpose

Skin Protectant

Topical Anesthetic

Skin Protectant

Uses

- Scar Management - Temporarily protects minor cuts , scrapes and burns

- Temporary relief of pain associated with minor cuts, scrapes and minor skin irritations

For external use only

Do not use

- on deep or puncture wounds, animal bites, serious burns

- in large quantities, particularly over raw surfaces or blistered areas

When using this product

- avoid contact with eyes

Stop use and ask a doctor if

- condition worsens, symptoms persist for more than 7 days or clear up and occur again within a few days

Keep out of reach of children. If pregnant or breastfeeding, contact physician prior to use

Directions

How to apply - clean and dry affected area - remove mesh from backing and apply to affected area

- use only one mesh at a time, and maximum of four mesh / day - leave mesh on affected area for up to

8 hours - children under 12 should consult

physician prior to use

Other information store below 25 C (77 F). avoid direct sunlight

For questions or concerns about this product, please call us - weekdays from 9 AM to 5 PM PST (1) 800-590-8070

RENUU NL 
allantoin, petrolatum patch
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:69329-011
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALLANTOIN (ALLANTOIN) ALLANTOIN 2 g  in 100 g
PETROLATUM (PETROLATUM) PETROLATUM 30 g  in 100 g
Inactive Ingredients
Ingredient Name Strength
.ALPHA.-TOCOPHEROL  
ONION  
Packaging
# Item Code Package Description
1 NDC:69329-011-15 15 PATCH in 1 BOX
1 NDC:69329-011-01 100 g in 1 PATCH
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 04/15/2014
Labeler - Patchwerx Labs (079584480)
Revised: 05/2015
 
Patchwerx Labs



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