Directions:
APPLY MEDICATION TO OILY AREA ONLY OF THE FACE IN VERY THIN LAYER. LEAVE ON OVERNIGHT.
Dr. Throwers Hydrotet
FDA Label NDC 69299-102
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dr. Thrower's Skincare, Inc. for the product Dr. Throwers Hydrotet (NDC 69299-102). 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 directions:, purpose:, ingredients:, warnings, 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
Purpose:
RX STRENGTH TOPICAL RETINOID FOR TREATMENT OF ACNE, SHAVING BUMPS, AND SPECIFIC BUMPY SKIN PROBLEMS. LEAVES SKIN SMOOTH, CLEAR AND NEW.
uSES: ACNE AND SPECIFIC SKIN CONDITIONS.
Ingredients:
Aqua, Ceteraryl Alcohol, Sodium Cetearyl Sulfate, Caprylic/Capric Triglyceride,Cyclopentasiloxane, Cyclohexasiloxane, Propylene Glycol, Alcohol Denatured, Decyl Oleate, Hydrogenated Elaesis Guineensis (Palm Kernal) Oil, Hydrogenated Glycine Soja (Soybean) Oil, Hydrogenated Gossypium Herbaceum (Cotton) Seed Oil, Lecithin, Diazolidinyl Urea , Methylparaben, Propylparaben, Tocopheryl Acetate, Disodium EDTA, Sodium Hyaluronate, Citric Acid , Aloe Barbadensis (Aloe) Leaf Juice
Warnings
STOP USE IF SKIN BECOMES IRRITATED (PINK, RED DARKER, OR EXCESSIVE PEELING). cONTACT DR. THROWER FOR INSTRUCTIONS. FOR EXTERNAL USE ONLY. KEEP OUT OF REACH OF CHILDREN. FEDERAL LAW PROHIBITS THE TRANSFER OF THIS DRUG TO ANY OTHER PERSON OTHER THAN FOR WHOM IT IS PRESCRIBED.
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