Otc - Active Ingredient
Minoxidil 5%
5% Minoxidil
FDA Label NDC 83889-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Lancity Information Technology Co., Ltd for the product 5% Minoxidil (NDC 83889-101). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, storage and handling, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Effective Solution
ForHair Thinning And Breakage
Make Hair Thicker Tealthier
Otc - Keep Out Of Reach Of Children
Keep out ofreach of children
Indications & Usage
1.Keep scalp clean and dry before use
2.Brush the hair and spray 6-7 times (about lml) on the scalp on the area of use
3.Massage the affected area for 3-5 minutes to allow the solution to absorb thoroughly
4.Wash hands after use to avoidcontamination with other items
Warnings
1.External use, not internal, avoiddirect contact with the eyes, such asaccidentallyinto the eyes, that is,wash with water ;
2. Keep out ofreach of children
3. If you feelunwell, stop using it.
Dosage & Administration
Brush the hair and spray 6-7 times (about lml) on the scalpon the area of use
Storage And Handling
Storage conditions: Please storein a cool and dry place to avoiddirect sunlight
Inactive Ingredient
Water
phenoxyethanol
turmeric extract
castor oil
ginseng extract
Package Label.Principal Display Panel
Label (Label)
Label2 (Label2)
* Please review the disclaimer below.
