Active Ingredient
Menthol 1.25%
Lactigo Gel
FDA Label NDC 72481-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Lactigo, Inc. for the product Lactigo (NDC 72481-101). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Topical analgesic
Use
For the temporary relief of minor aches and pains of muscles and joints.
Warnings
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
Keep out of reach of children to avoid accidental ingestion.
If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
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
Store at 15°C to 30°C (59°F to 86°F).
Inactive Ingredients
Ethoxydiglycol, glycerine, L-carnosine, magnesium sulfate, phenoxyethanol, water, xanthan gum
Questions?
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