Label: RENUU NL- allantoin, petrolatum patch
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Contains inactivated NDC Code(s)
NDC Code(s): 69329-011-01, 69329-011-15 - Packager: Patchwerx Labs
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated May 28, 2015
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- Official Label (Printer Friendly)
- INACTIVE INGREDIENT
- DESCRIPTION
- DESCRIPTION
- INDICATIONS & USAGE
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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
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INGREDIENTS AND APPEARANCE
RENUU NL
allantoin, petrolatum patchProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:69329-011 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 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:69329-011-15 15 in 1 BOX 1 NDC:69329-011-01 100 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)