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Dr. Throwers Pbc No. 1 Package Insert

Status:
Prescription (Rx) Facts
Strength:
12 g/100 g, 0.1 g/100 g, 0.5 g/100 g
Active ingredients:

Prescribing information (package insert) - Dr. Throwers Pbc No. 1

DIRECTIONS:

APPLY IN A VERY THIN LAYER IN THE DARK AREA ONLY. FOR DARK SPOTS APPLY TO THE CENTER OF DARK SPOTS.

FREQUENCY OF APPLICATION: DETERMINED BY DR. THROWER.

USES:

EXTREME SKIN DISCOLORATION AND DARK SPOTS.

INGREDIENTS:

Aqua, Ceteraryl Alcohol, Sodium Cetearyl Sulfate, Caprylic/Capric Triglyceride,Cyclopentasiloxane, Cyclohexasiloxane, Propylene Glycol, Butylene Glycol , Hydrogenated Lecithin,Sodium Oleate , Oligopeptide-68, Propanediol, Boerhavia Diffusa Root Extract ,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,Sodium Metabisulfite, 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). 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.

About this document

Source: FDA drug labeling via NLM DailyMed · View the label on DailyMed

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Drug information for Dr. Throwers Pbc No. 1

Rx or OTC
Prescription (Rx)?
  • This drug is available only with a prescription from a licensed healthcare provider.
  • Rx
Drug class Corticosteroid, Melanin Synthesis Inhibitor, Retinoid
Active ingredients Hydroquinone 12 g/100 g, Tretinoin 0.1 g/100 g, Betamethasone dipropionate 0.5 g/100 g
Dosage form Cream
Route Topical
Marketing status not in the current FDA NDC Directory
Company (applicant) DR. THROWER'S SKINCARE, INC.
FDA approval UNAPPROVED DRUG OTHERUnapproved drug
Manufacturers 1 labelers list this drug on DailyMed
Packages (NDC)
Package
12 g/100 g, 0.1 g/100 g, 0.5 g/100 g – 28 g in 1 jar NDC 69299-301-21

Source: FDA drug labeling via NLM DailyMed, data as of October 31, 2026. FDA data (DailyMed, Orange Book, Drug Shortages, enforcement reports). Not a substitute for the advice of a doctor or pharmacist.