Anti-Itch Cream
Anti-Itch Cream is an FDA drug label for the active ingredient ANTI-ITCH CREAM manufactured by Buzzie LLC administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260819.
- Generic name
- ANTI-ITCH CREAM
- Manufacturer
- Buzzie LLC
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 84051-001
- Application
- N/A
- Label effective
- 20260819
About this product
Anti-Itch Cream is an FDA-registered drug product whose active ingredient is ANTI-ITCH CREAM. It is labelled by Buzzie LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 84051-001, label effective 20260819. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing ANTI-ITCH CREAM are most often described in connection with: temporary relief, inflammation pain, itching burning, stinging sensation, based homeopathic, materia medica, clinical testing, product efficacy. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses For the temporary relief of inflammation, pain, itching, burning and stinging sensation. Indications are based on Homeopathic Materia Medica, not clinical testing. Product efficacy and claims are based on theories of homeopathy that are not supported by scientific evidence and most allopathic medical professionals. uses section
Dosage & Administration
Directions: Adults and children 2 years of age and older, apply a thin layer of cream on clean skin to cover the affected area • For best results, allow cream to be absorbed into the skin: do not rub in • Apply at the onset of symptoms, not more than 6 times daily or every 15 minutes for the first hour • Do not use with other topical remedies or lotions. directions
Warnings
Warning For external use only Do not use on damaged or broken skin Keep out of • eyes • open wounds • mucous membranes Stop use and ask a physician if • condition worsens or persist • rash develops Ask a physician before use if you are taking a prescription drug or have a serious medical condition If pregnant or breastfeeding consult your doctor before use Keep out of the reach of children If swallowed, get medical help or contact a Poison Control Center right away warning section
Recall and safety notices
5 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.
| Recall | Product | Firm | Class | Status | Reported |
|---|---|---|---|---|---|
| D-0427-2025 | Optim V, Anti-Itch Cream, Benzocaine 20% & Resorcinol 3% - External analgesic, Net Wt. Peso Neto 1 oz (28g) Tube, Distributed by: Pharmadel LLC, New Castle, DE 19720, Made in India, NDC 55758-300-01, UPC 8 59424 00420 6. | KENIL HEALTHCARE PRIVATE LIMITED | Class II | Terminated | 20250528 |
| D-0428-2025 | Rapidol Maximum Strength, Hydrocortisone 1% Anti-Itch Cream, NET WT 2 oz (60g) Tube, Distributed by: Pharmadel LLC, New Castle, DE, 19720, NDC 55758-420-02, UPC 8 10096 77158 2. | KENIL HEALTHCARE PRIVATE LIMITED | Class II | Terminated | 20250528 |
| D-1732-2019 | Hydrocortisone Cream With Aloe, Hydrocortisone 1% / Anti-Itch Cream with Aloe, 2 OZ (56 g) tube. Distributed By: Walgreen Co. 200 Wilmot Rd., Deerfield, IL 60015. NDC #0363-0620-04, UPC 3 11917 17934 6 | US Pharmaceuticals Inc. | Class II | Terminated | 20190821 |
| D-1734-2019 | Hydrocortisone Cream, Hydrocortisone 1% / Anti-Itch Cream, 2 OZ (56 g) tube. Distributed By: Walgreen Co. 200 Wilmot Rd., Deerfield, IL 60015. NDC #0363-0638-04, UPC 3 11917 18247 6 | US Pharmaceuticals Inc. | Class II | Terminated | 20190821 |
| D-1731-2019 | Hydrocortisone Cream With Aloe, Hydrocortisone 1% / Anti-Itch Cream with Aloe, 1 OZ (28 g) tube. Distributed By: Walgreen Co. 200 Wilmot Rd., Deerfield, IL 60015. NDC #0363-0620-03, UPC 3 11917 17935 3 | US Pharmaceuticals Inc. | Class II | Terminated | 20190821 |
Frequently asked questions
What is Anti-Itch Cream used for?
Uses For the temporary relief of inflammation, pain, itching, burning and stinging sensation. Indications are based on Homeopathic Materia Medica, not clinical testing. Product efficacy and claims are based on theories of homeopathy that are not supported by scientific evidence and most allopathic medical professionals. uses section
Who makes Anti-Itch Cream?
Buzzie LLC is the labeler of record for Anti-Itch Cream.
What form does Anti-Itch Cream come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Anti-Itch Cream prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has Anti-Itch Cream been recalled?
5 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.