Otc - Active Ingredient
Centella Asiatica Extract
Shynomore Lubricant
FDA Label NDC 72072-0001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bluette Co., Ltd. for the product Shynomore Lubricant (NDC 72072-0001). 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 otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Sodium Hyaluronate, Hamamelis Virginiana (Witch Hazel) Leaf Extract, etc.
Otc - Purpose
Water-soluble massage gel
Otc - Keep Out Of Reach Of Children
keep out or reach of the children
Indications & Usage
With clean hands, dispense an appropriate amount and apply on skin, massaging gently
Warnings
Precautions for Use
If any of the following conditions occur, discontinue use immediately and consult a dermatologist. Continuous use will cause symptoms to worsen.
1) In case of skin reaction such as red spots, swelling, itch or irritation etc. during use
2) In case of the above skin reaction when applied area is exposed to direct sunlight
Do not use on damaged skin area such as wound, rash or skin infection
Storage and Handling
1) Close lid tightly after use
2) Keep out of reach of infants and children
3) Store in a cool, dry place away from direct sunlight
4) Avoid eye area
Dosage & Administration
for external use only
Package Label.Principal Display Panel
1 (Label)
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