BLUE GOO NERVE EASE PAIN RELIEF TOPICAL ANALGESIC- lidocaine hcl 4%, menthol 1% liquid

blue goo NERVE EASE Pain RELIEF by

Drug Labeling and Warnings

blue goo NERVE EASE Pain RELIEF by is a Otc medication manufactured, distributed, or labeled by Garcoa, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient(s)

Lidocaine HCl 4%

Menthol 1%

Purpose

Topical analgesic

Topical analgesic

Use(s)

Use for the temporary relief of pain.

Warnings

WARNINGS

For External use only.

Do not use  in large quantities, particularly over raw surfaces or blistered areas  if you are allergic to lidocaine or other local anesthetics on damages, broken skin on cuts, swollen or irritated skin for more than a week without consulting a physician.

When using this product use only as directed avoid contact with the eyes do not use with heating pads, medicated patches or heating devices do not bandage tightly read and follow all directions and warnings on this carton avoid applying into skin folds do not apply over large areas of the body a slight burning sensation may occur upon application but usually disappears in several days.

Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days pain, swelling, blistering develops where product is used redness, rash, itching, irritation develops where product is used.

Flammable keep away from fire or flame.

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 a Poison Control Center (1-800-222-1222) immediately.

For external use only

Do not use

Ask a doctor before use if

Ask a doctor or pharmacist before use if

When using this product

Stop use and ask a doctor if

Pregnancy/Breastfeeding

Keep out of reach of children

Directions

Directions Adults and children 12 years age and older  clean and dry affected area apply a thin layer to affected area not more than 3 times daily do not apply more than three times within 24 hours massage into painful area until thoroughly absorbed into the skin wash hands after use with soap and water. Children under 12 years of age: do not use, consult a doctor.

Inactive ingredients

Inactive ingredients acrylates/Cl10-30 alkyl acrylate crosspolymer, alcohol denat.,
aminomethyl propanol, C30-45 alkyl cetearyl dimethicone crosspolymer, caprylyl methicone,
cetearyl alcohol, ceteth-20 phosphate, dicetyl phosphate, dimethicone, disodium EDTA,
ethylhexylglycerin, glyceryl stearate, hydroxyethyl acrylate/sodium acryloyldimethyl taurate
copolymer, isohexadecane, phenoxyethanol, polysorbate 60, steareth-21, water.

Questions

Question or comments? 1866-567-8600

SPL UNCLASSIFIED SECTION

BLUE GOO PRODUCTS

div. of GARCOA LABS

Calabasas, CA 91302

Principal Display Panel

blue goo

NERVE EASE 

Pain 

RELIEF

4% LIDOCAINE HCl

1% MENTHOL

PAIN RELIEVING LIQUID

ROLL-ON

Helps to Penetrate for Targeted,

Numbing Nerve Pain Relief

2.5 FL OZ (74mL)

INGREDIENTS AND APPEARANCE

BLUE GOO NERVE EASE PAIN RELIEF  TOPICAL ANALGESIC
lidocaine hcl 4%, menthol 1% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67385-825
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	40 mg  in 1 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S AT 0.5%) (UNII: YY2HMJ9NZF)
ALCOHOL (UNII: 3K9958V90M)
AMINOMETHYL PROPANOL (UNII: LU49E6626Q)
C30-45 ALKYL CETEARYL DIMETHICONE CROSSPOLYMER (UNII: 4ZK9VP326R)
CAPRYLYL METHICONE (UNII: Q95M2P1KJL)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
CETETH-20 PHOSPHATE (UNII: 921FTA1500)
DICETYL PHOSPHATE (UNII: 2V6E5WN99N)
DIMETHICONE (UNII: 92RU3N3Y1O)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
ISOHEXADECANE (UNII: 918X1OUF1E)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 60 (UNII: CAL22UVI4M)
STEARETH-21 (UNII: 53J3F32P58)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67385-825-01	1 in 1 CARTON	08/27/2025
1		74 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M014	08/27/2025

Labeler - Garcoa, Inc. (036464697)

Registrant - Garcoa, Inc. (036464697)