Active Ingredient
Salicylic Acid 3%
Folliculitis Scalp Spray
FDA Label NDC 83004-013
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Rida Llc for the product Folliculitis Scalp (NDC 83004-013). 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 active ingredient, purpose, uses, warnings, directions, other information, inactive ingredients, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
- Minimizes scalp irritation and itching
Uses
- Specifically formulated for the treatment of scalp folliculitis.
- Provides relief from symptoms associated with folliculitis on the scalp.
- Helps reduce redness, itching, and discomfort caused by inflamed hair follicles on the scalp.
Warnings
- For external use only.
- Do not apply to broken skin or open wounds.
- Discontinue use if irritation or rash occurs.
- Keep out of reach of children.
- If pregnant or breastfeeding, consult a healthcare professional before use.
Directions
- Shake well before use.
- Apply the Folliculitis Scalp Spray to the affected area 2–3 times daily.
- Avoid contact with eyes and mucous membranes.
- If symptoms persist or worsen, consult a healthcare provider.
Other Information
- Store in a cool, dry place. Protect from direct sunlight.
Inactive Ingredients
Aqua (Water), Trehalose, Benzalkonium Chloride, Mirtazapine, Hexamidine, Sodium Hyaluronate, Salvia Miltiorrhiza Extract, Ginkgo Biloba Extract, Bacillus Subtilis Ferment, Coptis Chinensis Extract, 1,2-Hexanediol, Hydroxypropyl Guar, Saponins, Apple Cider Vinegar
Product Label
Image Description (Label1)
Image Description (Label2)
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