BLUE GOO PAIN RELIEVING- menthol 2.5% gel

blue goo Pain Relieving by

Drug Labeling and Warnings

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

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Menthol 2.5%

Purpose

• Topical Analgesic

Uses

For the temporary relief of muscle aches, pains and strains, arthritic pain, joint pain, and tendonitis

Warnings

For external use only

Avoid contact with eyes Do not apply to wounds or damaged skin Do not bandage tightly Do not use with heating pads or heating devices Discontinue use and consult a doctor if condition worsens or if symptoms persist for 7 days or more or clear up and occur again within a few days, or if pain, swelling or redness occurs after continued use

Directions

Directions

Adults and children 6 years of age and older apply liberally to affected area not more than 3-4 times daily. Children under 6 years of age: Do Not Use.

Inactive ingredients

water, dimethyl sulfone, emu oil, alcohol denat., sodium chondroitin sulfate, glucosamine HCl, camphor, chrysanthemum parthenium (Feverfew) extract,  arnica montana flower extract, chamomilla recutita (Matricaria) flower extract, urtica dioica (Nettle) extract, hamamelis virginiana (Witch Hazel) extract, calendula officinalis extract, salix alba (Willow) bark extract, coriandrum sativum (Coriander) extract, aloe barbadensis leaf juice, eucalyptus globulus leaf oil, fragrance, sodium hydroxide, carbomer, sorbitol, methyl salicylate, phenoxyethanol, blue 1

Questions or comments

1-866-567-8600

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PDP

Blue Goo Pain

INGREDIENTS AND APPEARANCE

BLUE GOO PAIN RELIEVING 
menthol 2.5% gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67385-883
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	2.5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
EMU OIL (UNII: 344821WD61)
DEHYDRATED ALCOHOL (UNII: 3K9958V90M)
GLUCOSAMINE HCL (UNII: 750W5330FY)
SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
FEVERFEW (UNII: Z64FK7P217)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ)
URTICA DIOICA FLOWER (UNII: 9B7Z94PNQ5)
WITCH HAZEL (UNII: 101I4J0U34)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
WILLOW BARK (UNII: S883J9JDYX)
CORIANDER (UNII: 1OV56052IK)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
EUCALYPTUS GLOBULUS LEAF OIL (UNII: 2R04ONI662)
FRAGRANCE 13576 (UNII: 5EM498GW35)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
CARBOMER (UNII: 0A5MM307FC)
SORBITOL (UNII: 506T60A25R)
METHYL SALICYLATE (UNII: LAV5U5022Y)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BLUE 1 (UNII: H3R47K3TBD)

Product Characteristics
Color	blue	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67385-883-01	113 g in 1 JAR; Type 0: Not a Combination Product	01/17/2025
2	NDC: 67385-883-02	907 g in 1 BOTTLE; Type 0: Not a Combination Product	01/17/2025
3	NDC: 67385-883-03	453.6 g in 1 BOTTLE; Type 0: Not a Combination Product	01/05/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	01/17/2025

Labeler - Garcoa, Inc. (036464697)