Uses
ECZEMA, SPECIFIC DRY SKIN, AND SPECIFIC SKIN IRRITATIONS.
Dr. Throwers Beta
FDA Label NDC 69299-201
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 Beta (NDC 69299-201). 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 uses, directions:, 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
Directions:
APPLY MEDICATION TO AREA OF SKIN IRRITATION IN A VERY THIN LAYER. LEAVE ON OVERNIGHT.
FREQUENCY OF APPLICATION: DETERMINED BY DR. THROWER.
Ingredients:
AQUA, CETEARYL ALCOHOL, SODIUM CETEARYL SULFATE, CAPRYLIC/CAPRIC TRIGLYCERIDES, CYCLOPENTASILOXANE, CYCLOHEXASILOXANE, PROPYLENE GLYCOL, ALCOHOL DENATURED, DECYL OLEATE, HYDROGENATED ELAESIS GUINEENSIS (PALM KERNEL) OIL, HYDROGENATED GLYCINE SOYA (SOYBEAN) OIL, HYDROGENATED GOSSYPIUM HERBACEUM (COTTON) SEED OIL, LECITHIN, DIAZOLYDINYL 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 PRESCRIBED.
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