Label: EB301CT BRUISE PAIN RELIEF- menthol spray
-
Contains inactivated NDC Code(s)
NDC Code(s): 53304-1301-1 - Packager: EMINENCE BIOTECH CORPORATION LIMITED
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 March 20, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 100 mL Bottle Carton
-
INGREDIENTS AND APPEARANCE
EB301CT BRUISE PAIN RELIEF
menthol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53304-1301 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM 1700 mg in 100 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) AMARANTHUS VIRIDIS LEAF (UNII: 7T0WZ76K1T) PORK SIDE BACON, CURED FAT (UNII: 6E710H379S) GAULTHERIA PROCUMBENS LEAF (UNII: 2125M16OWN) GLYCERIN (UNII: PDC6A3C0OX) EUPHORBIA THYMIFOLIA WHOLE (UNII: D56Y3D2OTL) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53304-1301-1 1 in 1 BOX 03/01/2013 1 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part348 03/01/2013 Labeler - EMINENCE BIOTECH CORPORATION LIMITED (078531141)