Health Care Function
Relieve neck, shoulder, waist, leg pain and promote health
Wormwood Patch
FDA Label NDC 84727-013
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Baishili Trading Co., Ltd for the product Wormwood Patch (NDC 84727-013). 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 health care function, usage, matters needing attention, unsuitable people, keep out of reach of children., dosage & administration section, inactive ingredient section, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Usage
Opened the package back lining paper torn off，clean your skin where the discomfort,aim at the knee or discomfort parts were applied，the corresponding around six to eight hours per post.
Matters Needing Attention
1. The skin lesions were banned, allergic to wormwood careful.
2. During the period of a few people use local have tickling feeling or a red rash,does not afect theuse disappeared gradually after stopping
3. The use of skin burns is a normal phenomenon.
Unsuitable People
Pregnant women, those allergic to wormwood are prohibited
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away
Dosage & Administration Section
Apply one piece at a time, and each piece should be applied for 8 hours
Inactive Ingredient Section
Peppermint 50%
Dosage & Administration
Medical glue 40%
Far infrared ceramic powder 5%
Magnetic Powder 5%
Package Label.Principal Display Panel
Label-01 (Label 01)
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