NDC | 69329-012-01, 69329-012-15 |
Set ID | 1719195f-7e34-1489-e054-00144ff88e88 |
Category | HUMAN PRESCRIPTION DRUG LABEL |
Packager | Patchwerx Labs |
Generic Name | |
Product Class | Amide Local Anesthetic, Antiarrhythmic |
Product Number | |
Application Number |
- INACTIVE INGREDIENT
- DESCRIPTION
- DESCRIPTION
- INDICATIONS & USAGE
-
WARNINGS
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
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
RENUU PATCH
allantoin, lidocaine, petrolatum patchProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:69329-012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 2 g in 100 g LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 5 g in 100 g PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 30 g in 100 g Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) ONION (UNII: 492225Q21H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69329-012-15 15 in 1 BOX 1 NDC:69329-012-01 100 g in 1 PATCH; Type 0: Not a Combination Product 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)