Palm
Palm is an FDA drug label for the active ingredient CHLOROXYLENOL manufactured by ABC Compounding Co., Inc. 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 20260511.
- Generic name
- CHLOROXYLENOL
- Manufacturer
- ABC Compounding Co., Inc.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 62257-544
- Application
- M003
- Label effective
- 20260511
About this product
Palm is an FDA-registered drug product whose active ingredient is CHLOROXYLENOL. It is labelled by ABC Compounding Co., Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 62257-544, application M003, label effective 20260511. It is one of 45 FDA drug label records sharing the active ingredient CHLOROXYLENOL. 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 CHLOROXYLENOL are most often described in connection with: drug facts, box otc-indications, usage section, hand-washing decrease. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Drug Facts Box OTC-Indications & Usage Section for hand-washing to decrease bacteria on the skin
Dosage & Administration
Drug Facts Box OTC-Dosage & Administration Section wet hands and forearms apply 5 milliliters (teaspoonful) or palmful to hands and forearms scrub thoroughly for 1 minute and rinse
Warnings
Drug Facts Box OTC-Warnings Section For external use only
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View labelHow products containing CHLOROXYLENOL compare
FDA lists 45 drug label records with CHLOROXYLENOL as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | ABC Compounding Co., Inc. | 6 |
| — | — | CODAA SWITZERLAND AG | 4 |
| — | — | Avro Enterprises LLC | 2 |
| — | — | CODAA Switzerland AG | 2 |
| — | — | Fuller Industries, Inc | 2 |
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-0006-2027 | Sterile Lubricant Dry Eye Relief Eye Drops, 0.5 FL OZ (15 mL); a) LEADER, DISTRIBUTED BY CARDINAL HEALTH, DUBLIN, OHIO 43017, www.myleader.com, NDC 70000-0502-1; b) Crocodile Tears, Distributed by: Crocodile Tears, Palm Beach Gardens, FL 33410, UPC: 8 67166 00000 4; c) Discount drug mart, Discount Drug Mart Food Fair, Medina, OH 44256, UPC: 0 93351 01156 6; d) exchange select, Manufactured for your Military Exchange By: K.C Pharmaceuticals, Inc., Pomona, CA 9176, UPC: 6 14299 05620 6; e) GERI CARE, Distributed by: Gericare Pharmaceuticals Corp., 1295 Towbin Ave., Lakewood, NJ 08701, NDC 57896-181-05; f) H.E.B Dry Eye, Eye Drops, MADE WITH PRIDE & CARE FOR H-E-B, SAN ANTONIO, TX 78204, UPC 0 41220 43741 2; g) Harris Teeter, PROUDLY DISTRIBUTED BY: HARRIS TEETER, LLC, MATTHEWS, NC 28105, UPC: 0 72036 71303 2; h) Foster & Thrive, Distributed by: McKesson Corp. Via Strategic Sourcing Servies LLC., Memphis, TN 38141, NDC 70677-1157-1; I) TopCare health, DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELKGROVE VILLAGE, IL 60007, UPC 0 36800 36100 3. | K.C. Pharmaceuticals, Inc. | Class II | Ongoing | 20261014 |
| D-0768-2026 | CLINDAMYCIN PALMITATE HYDROCHLORIDE FOR ORAL SOLUTION, USP, 75 mg/5 mL, Rx Only, 100 mL, Distributed by: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816, NDC 23155-603-51 | Heritage Pharmaceuticals Inc | Class II | Ongoing | 20260819 |
| D-0627-2026 | Povi-One, 10% Povidone-Iodine Oral Antiseptic, Packaged by Elevate Oral Care, LLC, 346 Pike Road, Suite 6, West Palm Beach, FL 33411, NDC 57511-0611-1. | Elevate Oral Care | Class II | Ongoing | 20260701 |
| D-0191-2026 | Karina Daily Moisturizer SPF 25, Octinoxate 7.5% and Zinc Oxide 7.0%, Net WT. 5 oz/ 141.7 g per tube, Dist. By: Beauty4Pros LLC, Palm Desert, CA 92211. NDC: 35192-033-16, UPC 8 18204 02572 5 | CA BOTANA International, Inc. | Class II | Ongoing | 20251203 |
| D-0196-2026 | Dr. Bump Natural Pain Relief Gel, Menthol 5%, NET WT 4 FL OZ/118 ML per bottle, Distr. by 1Beauty US LLC, Palm Desert, CA 92211. NDC: 35192-052-18, UPC 8 18204 02513 8 | CA BOTANA International, Inc. | Class II | Ongoing | 20251203 |
Frequently asked questions
What is Palm used for?
Drug Facts Box OTC-Indications & Usage Section for hand-washing to decrease bacteria on the skin
Who makes Palm?
ABC Compounding Co., Inc. is the labeler of record for Palm. 45 FDA label records share the active ingredient CHLOROXYLENOL, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.
What form does Palm 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 Palm 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.
Are there other products containing CHLOROXYLENOL?
Yes. 45 FDA drug label records list CHLOROXYLENOL as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.
Has Palm 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.