LactiGo with Menthol Performance & Recovery Gel

Manufacturer: LactiGo, Inc.
Effective date: 2024-09-03
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 00:18:46

Label at a glance#

ProductLactiGo

Active ingredientMENTHOL, UNSPECIFIED FORM

Label structure10 sections

Dosage and administration

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: Consult a doctor.

Storage and handling

Store at 15°C to 30°C (59°F to 86°F).

Contacts and useful links#

PhoneLabel contact1-844-522-8446

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 1.25%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Use

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints.

Warnings

WARNINGS SECTION

For external use only.

Avoid contact with eyes and mucous membranes.
If contention worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor.
Do not apply to wounds or damaged skin.
Do not bandage tightly.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children to avoid accidental ingestion.

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

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.

Children under 2 years of age: Consult a doctor.

Other information

STORAGE AND HANDLING SECTION

Store at 15°C to 30°C (59°F to 86°F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Ethoxydiglycol, glycerine, L-carnosine, magnesium sulfate, phenoxyethanol, water, xanthan gum

Questions?

OTC - QUESTIONS SECTION

1-844-522-8446

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label_100

label_946

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
866128	menthol 1.25 % Topical Gel	PSN	4
866128	menthol 0.0125 MG/MG Topical Gel	SCD	4
866128	menthol 1.25 % Topical Gel	SY	4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
95250459-30e4-45c1-b08a-993044f49109	Product name	2	20250805
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
9badc7be-250a-44ab-aa36-926af3f02679	Product name	1	20210527
26acd337-b838-40ac-bcbc-05c3b81c8712	Product name	1	20170323

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72481-101-03	LactiGo	100 mL in 1 BOTTLE, PUMP	GEL	100		4
72481-101-32	LactiGo	946 mL in 1 BOTTLE, PUMP	GEL	946		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72481-101	LACTIGO (MENTHOL) GEL [LACTIGO, INC.]	4	Current NDC, Legacy NDC, 2 package rows	20240905_849c3601-2bc8-0991-e053-2a91aa0a5e7f.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

LactiGo
MENTHOL
MAGNESIUM SULFATE ANHYDROUS
DIETHYLENE GLYCOL MONOETHYL ETHER
WATER
CARNOSINE
XANTHAN GUM
PHENOXYETHANOL
MENTHOL, UNSPECIFIED FORM
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72481-101	72481-101-03, 72481-101-32

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MAGNESIUM SULFATE ANHYDROUS	ML30MJ2U7I	IACT
DIETHYLENE GLYCOL MONOETHYL ETHER	A1A1I8X02B	IACT
WATER	059QF0KO0R	IACT
CARNOSINE	8HO6PVN24W	IACT
XANTHAN GUM	TTV12P4NEE	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
MENTHOL, UNSPECIFIED FORM	L7T10EIP3A	ACTIB
GLYCERIN	PDC6A3C0OX	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
LactiGo	MENTHOL	LactiGo, Inc.	849c3601-2bc8-0991-e053-2a91aa0a5e7f	2024-09-03	Warnings	Exact identifier ndc (package): 72481-101-32 ndc (package): 72481-101-03 ndc (product): 72481-101 ndc11 (package): 72481010132 ndc11 (package): 72481010103 spl id: 213e8489-762b-461f-e063-6394a90a64a3 spl set id: 849c3601-2bc8-0991-e053-2a91aa0a5e7f

Reported adverse events (FAERS/openFDA)#

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