BLUE-EMU LIDOCAINE PAIN RELIEF CREAM- lidocaine cream 4% cream 
NFI, LLC

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Blue-Emu ®Lidocaine Pain Relief Cream

Active Ingredients

Lidocaine HCl 4%

Purpose

Topical anesthetic

Uses

temporarily relieves minor pain

Warnings

For external use only

Do not use

  • on large areas of the body or on cut, irritated or swollen skin
  • on puncture wounds
  • for more than one week without consulting a doctor

When using this product

  • use only as directed. Read and follow all directions and warnings on this carton.
  • do not allow contact with the eyes
  • do not bandage or apply local heat (such as heating pads) to the area of use

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

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

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

Directions

Adults and children over 12 years:

Children 12 years or younger:ask a doctor

Inactive Ingredients

acrylates acrylamide copolymer, aloe barbadensis leaf juice (aloe vera), allantoin, caprylic capric triglyceride, cetyl alcohol, dl-panthenol, dimethicone, ethylhexylglycerin, emu oil, glycerin, glyceryl stearate, mineral oil, phenoxyethanol, polyethylene glycol 100 stearate, polysorbate 80, polysorbate 85, sodium polycrylate, stearic acid, triethanolamine, tocopherol acetate (Vitamin E), water.

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

Product label

image description

BLUE-EMU LIDOCAINE PAIN RELIEF CREAM 
lidocaine cream 4% cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69993-350
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS40 mg
Inactive Ingredients
Ingredient NameStrength
CETYL ALCOHOL (UNII: 936JST6JCN)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
WATER (UNII: 059QF0KO0R)  
CAPRYLIC/CAPRIC/LINOLEIC TRIGLYCERIDE (UNII: U73D397055)  
PANTHENOL (UNII: WV9CM0O67Z)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
EMU OIL (UNII: 344821WD61)  
GLYCERIN (UNII: PDC6A3C0OX)  
PEG-120 GLYCERYL STEARATE (UNII: 6941286E4I)  
MINERAL OIL (UNII: T5L8T28FGP)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
POLYSORBATE 85 (UNII: A7F3N56197)  
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALLANTOIN (UNII: 344S277G0Z)  
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69993-350-031 in 1 CARTON03/01/2017
177 in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01703/01/2017
Labeler - NFI, LLC (121681919)
Establishment
NameAddressID/FEIBusiness Operations
Gregory Pharmaceutical Holdings, Inc., dba UPM Pharmaceuticals081301372manufacture(69993-350)

Revised: 5/2024
Document Id: 18a9fab7-c397-3905-e063-6394a90adf49
Set id: 592811f2-e21c-6a58-e053-2991aa0a69a9
Version: 9
Effective Time: 20240517
 
NFI, LLC