Label: MAXIMUM STRENGTH BLUE EMU PAIN RELIEF BLU EMU- trolamine salicylate spray
- NDC Code(s): 69993-100-04
- Packager: NFI, LLC
- 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 May 4, 2023
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
Allergy alert:
If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.
When using this product
- •
- use only as directed
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- do not bandage tightly or use with a heating pad
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- avoid contact with eyes or mucous membranes
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- do not apply to wounds or damaged skin.
- Directions
- Inactive ingredients
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 118 ml Can Label
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INGREDIENTS AND APPEARANCE
MAXIMUM STRENGTH BLUE EMU PAIN RELIEF BLU EMU
trolamine salicylate sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69993-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Trolamine Salicylate (UNII: H8O4040BHD) (Salicylic Acid - UNII:O414PZ4LPZ) Trolamine Salicylate 10 g in 100 mL Inactive Ingredients Ingredient Name Strength Aloe (UNII: V5VD430YW9) Caprylyl Glycol (UNII: 00YIU5438U) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) Edetate Disodium (UNII: 7FLD91C86K) DMDM Hydantoin (UNII: BYR0546TOW) Emu Oil (UNII: 344821WD61) Glucosamine Sulfate (UNII: 1FW7WLR731) Glycerin (UNII: PDC6A3C0OX) GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) Oleic Acid (UNII: 2UMI9U37CP) Panthenol (UNII: WV9CM0O67Z) Phenoxyethanol (UNII: HIE492ZZ3T) Polysorbate 20 (UNII: 7T1F30V5YH) SORBITOL (UNII: 506T60A25R) Water (UNII: 059QF0KO0R) Xanthan Gum (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69993-100-04 118 mL in 1 CAN; Type 0: Not a Combination Product 06/04/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 06/04/2012 Labeler - NFI, LLC (121681919) Establishment Name Address ID/FEI Business Operations Formulated Solutions, LLC 143266687 MANUFACTURE(69993-100)