BLUE-EMU MAXIMUM ARTHRITIS PAIN RELIEF CREAM- trolamine salicylate 10% cream 
Gregory Pharmaceutical Holdings, Inc., dba NFI Consumer Products

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.

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NFI Consumer Products Blue-Emu Maximum Arthritis Pain Relief Cream

Active Ingredient

Trolamine salicylate 10%

Purpose

Topical analgesic

Uses

Temporarily relieves minor pain associated with:

arthritis
simple backache
muscle strains
sprains
bruises
cramps

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
do not bandage tightly or use with a heating pad
avoid contact with eyes or mucos membranes
do not apply to wounds or damaged skin

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
redness is present
irritation develops

If pregnant or breast-feeding

ask a health professional before use.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adults and children over 12 years of age:

​apply generously to affected area
massage into painful area until thoroughly absorbed into skin
repeat as necessary, but no more than 4 times daily

Children 12 years or younger:

ask a doctor

Inactive Ingredients

acrylates/c10-30 alkyl acrylate crosspolymer, allantoin, aloe barbadensis leaf juice(Aloe Vera), cetyl alcohol, d-glucosamine, dimethicone, disodium EDTA, d- panthenol, emu oil, ethylhexylglycerin, F D & C Blue#1, glycerin, glyceryl stearate and peg-100 stearate, methylsulfonylmethane, mineral oil, phenoxyethanol, polysorbate 80, stearic acid, triethanolamine, tocopherol acetate(Vitamin E ), water.

Tube Image
BLUE-EMU MAXIMUM ARTHRITIS PAIN RELIEF CREAM 
trolamine salicylate 10% cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69993-250
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TROLAMINE SALICYLATE (UNII: H8O4040BHD) (SALICYLIC ACID - UNII:O414PZ4LPZ) TROLAMINE SALICYLATE100 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALLANTOIN (UNII: 344S277G0Z)  
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYETHYLENE GLYCOL 4500 (UNII: TVH7653921)  
MINERAL OIL (UNII: T5L8T28FGP)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
GLUCOSAMINE (UNII: N08U5BOQ1K)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
PANTHENOL (UNII: WV9CM0O67Z)  
EMU OIL (UNII: 344821WD61)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Product Characteristics
ColorblueScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69993-250-0388 g in 1 TUBE; Type 0: Not a Combination Product06/01/201508/31/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34806/01/201508/31/2020
Labeler - Gregory Pharmaceutical Holdings, Inc., dba NFI Consumer Products (118228461)

Revised: 2/2022
 
Gregory Pharmaceutical Holdings, Inc., dba NFI Consumer Products