Blue-Emu Pain Relief Micro-Foam

Manufacturer: Kingsway Pharmaceuticals dba NFI, LLC | Formulated Solutions, LLC
Effective date: 2025-12-05
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: monthly-update
Hydrated at: 2026-06-03 17:45:43

Label at a glance#

ProductBlue-Emu Pain Relief Micro-Foam

Active ingredientTROLAMINE SALICYLATE

Label structure9 sections

Indications and uses

temporarily relieves minor pain associated with: • arthritis • simple backache • muscle strains • sprains • bruises • cramps

Dosage and administration

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.

Contacts and useful links#

PhoneLabel contact1-800-432-9334

Websitewww.blue-emu.com

WWW.BLUE-EMU.COM

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Trolamine salicylate 10%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Uses

INDICATIONS & USAGE SECTION

temporarily relieves minor pain associated with:

arthritis
simple backache
muscle strains
sprains
bruises
cramps

Warnings

WARNINGS SECTION

For external use only

Allergy alert:

SPL UNCLASSIFIED SECTION

If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.

When using this product

OTC - WHEN USING SECTION

use only as directed
do not bandage tightly or use with a heating pad
avoid contact with eyes or mucous membranes
do not apply to wounds or damaged skin.

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens
symptoms persist for more than 7 days or clear up and occur again within a few days
redness is present
irritation develops.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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.

Other information

OTHER SAFETY INFORMATION

Store at 68-77^oF (20-25^oC)

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

SPL UNCLASSIFIED SECTION

DISTRIBUTED BY:
NFI CONSUMER PRODUCTS
501 Fifth Street • Bristol, TN 37620
TOLL FREE: 1-800-432-9334
WWW.BLUE-EMU.COM

PRINCIPAL DISPLAY PANEL – Canister Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SOFT & SOOTHING

BLUE-EMU^®

Fast Acting
Odor Free
+ Emu Oil

Pain Relief
Micro-Foam™

AMERICA'S
# 1
ODOR
FREE
EMU OIL FORMULA

Contains Emu Oil
NET WT 3.5 OZ (99.2g)

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 25 matching rows.

Blue-Emu Pain Relief Micro-Foam
TROLAMINE SALICYLATE
SALICYLIC ACID
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
ALLANTOIN
ALOE VERA LEAF
CETYL ALCOHOL
DIMETHICONE, UNSPECIFIED
EDETATE DISODIUM ANHYDROUS
EMU OIL
ETHYLHEXYLGLYCERIN
FD&C BLUE NO. 1
GLUCOSAMINE
GLYCERIN
GLYCERYL STEARATE/PEG-100 STEARATE
DIMETHYL SULFONE
MINERAL OIL
NITROUS OXIDE
PANTHENOL
PHENOXYETHANOL
POLYSORBATE 80
STEARIC ACID
TROLAMINE
.ALPHA.-TOCOPHEROL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69993-500	69993-500-35

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
TROLAMINE SALICYLATE	H8O4040BHD	ACTIB
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
ALLANTOIN	344S277G0Z	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
CETYL ALCOHOL	936JST6JCN	IACT
DIMETHICONE, UNSPECIFIED	92RU3N3Y1O	IACT
EDETATE DISODIUM ANHYDROUS	8NLQ36F6MM	IACT
EMU OIL	344821WD61	IACT
ETHYLHEXYLGLYCERIN	147D247K3P	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
GLUCOSAMINE	N08U5BOQ1K	IACT
GLYCERIN	PDC6A3C0OX	IACT
GLYCERYL STEARATE/PEG-100 STEARATE	RD25J5V947	IACT
DIMETHYL SULFONE	9H4PO4Z4FT	IACT
MINERAL OIL	T5L8T28FGP	IACT
NITROUS OXIDE	K50XQU1029	IACT
PANTHENOL	WV9CM0O67Z	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
POLYSORBATE 80	6OZP39ZG8H	IACT
STEARIC ACID	4ELV7Z65AP	IACT
TROLAMINE	9O3K93S3TK	IACT
.ALPHA.-TOCOPHEROL	H4N855PNZ1	IACT
WATER	059QF0KO0R	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
bd71b4dd-adf2-4ff6-bf25-3ea033420f3e			7fbcae35-e538-41a6-a826-518dd1c05fec	2025-12-05	Warnings	Exact identifier spl id: bd71b4dd-adf2-4ff6-bf25-3ea033420f3e spl set id: 7fbcae35-e538-41a6-a826-518dd1c05fec

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.