Label: BURN RELIEFRELIEF- lidocaine 0.5% spray
-
Contains inactivated NDC Code(s)
NDC Code(s): 41250-540-04 - Packager: Meijer
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated July 20, 2018
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient Purpose
- PURPOSE
- Uses
- Warnings
- Directions
- Inactive ingredients
- Questions? 866-483-2846
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
BURN RELIEFRELIEF
lidocaine 0.5% sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-540 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Lidocaine (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) Lidocaine 0.5 g in 100 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) Diazolidinyl Urea (UNII: H5RIZ3MPW4) Disodium Cocoamphodipropionate (UNII: 6K8PRP397M) EDETATE DISODIUM (UNII: 7FLD91C86K) Glycerin (UNII: PDC6A3C0OX) Methylparaben (UNII: A2I8C7HI9T) Propylene Glycol (UNII: 6DC9Q167V3) Propylparaben (UNII: Z8IX2SC1OH) ALCOHOL (UNII: 3K9958V90M) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TROLAMINE (UNII: 9O3K93S3TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-540-04 127 g in 1 CAN; Type 0: Not a Combination Product 10/06/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 10/06/2011 Labeler - Meijer (006959555) Registrant - Product Quest Mfg (927768135) Establishment Name Address ID/FEI Business Operations Product Quest Mfg 927768135 manufacture(41250-540) , label(41250-540)