Axe
Axe is an FDA drug label for the active ingredient BLACK FROZEN PEAR AND CEDARWOOD 48H SWEAT AND ODOR PROTECTION ANTIPERSPIRANT DEODORANT STICK manufactured by Conopco, Inc. d/b/a Unilever 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 20260707.
- Generic name
- BLACK FROZEN PEAR AND CEDARWOOD 48H SWEAT AND ODOR PROTECTION ANTIPERSPIRANT DEODORANT STICK
- Manufacturer
- Conopco, Inc. d/b/a Unilever
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 64942-2397
- Application
- M019
- Label effective
- 20260707
About this product
Axe is an FDA-registered drug product whose active ingredient is BLACK FROZEN PEAR AND CEDARWOOD 48H SWEAT AND ODOR PROTECTION ANTIPERSPIRANT DEODORANT STICK. It is labelled by Conopco, Inc. d/b/a Unilever taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 64942-2397, application M019, label effective 20260707. 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 BLACK FROZEN PEAR AND CEDARWOOD 48H SWEAT AND ODOR PROTECTION ANTIPERSPIRANT DEODORANT STICK are most often described in connection with: reduces underarm. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
reduces underarm wetness
Dosage & Administration
apply to underarms only
Warnings
For external use only. Do not use on broken skin. Stop use if rash or irritation occurs. Ask a doctor beforeuse if you have kidney disease.
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-0286-2026 | Deodorant: a) Axe, Body Spray, Wild Spice, 6CT, 150ML, UPC: 600108736469; b) LUCKY MENS STICK DEODORANT, SPRING FRESH, 24CT, 2.5 OZ, UPC: 808829111668; c) LUCKY MENS STICK DEODORANT, FRESH COMFORT, 24CT, 1.6 OZ, UPC: 808829089103; d) LADY DEODORANT, CHERRY BLOSSOSM, 24CT, 1.8oz, UPC: 048155921092; e) AXE, BODY SPRAY, APOLLO, 6CT, 150ML; f) AXE, BODY SPRAY, BLACK, 6CT, 150ML; g) AXE, BODY SPRAY, DARK TEMPTATION, 6CT, 150ML; h) AXE, BODY SPRAY, GOLD, 6CT, 150ML; i) AXE, BODY SPRAY, EXCITE, 6CT, 150ML; j) AXE, BODY SPRAY, ICE CHILL, 6CT, 150ML; k) AXE, BODY SPRAY, MUSK, 6CT, 150ML; l) AXE, DEODORANT SPRAY, ADRENALIN, 6CT, 150ML | GOLD STAR DISTRIBUTION INC | Class II | Ongoing | 20260121 |
| D-0007-2025 | Pluvicto, 1000 MBq/mL (27 mCi/mL), lutetium, LU 177, vipivotide tetraxetan injection, Single-dose vial, Sterile, Manufacturer Advanced Accelerator Applications, 57 E. Willow Street, NJ 07041, Millburn USA. NDC 69488-0010-61 | Advanced Accelerator Applications USA, Inc. | Class II | Ongoing | 20241009 |
| D-0554-2024 | Docetaxel Injection, USP, 160 mg per 16 mL (10 mg per mL), 1 x 16 mL Multi-Dose Vial, Rx only, Mfd. for Sagent Pharmaceuticals, Schaumburg, IL 60195 (USA), Made in India. NDC 25021-254-08 | Sagent Pharmaceuticals | Class I | Ongoing | 20240619 |
| D-0553-2024 | Docetaxel Injection, USP, 80 mg per 8 mL (10 mg per mL), 1 x 8 mL Multi-Dose Vial, Rx only, Mfd. for Sagent Pharmaceuticals, Schaumburg, IL 60195 (USA), Made in India. NDC 25021-254-08 | Sagent Pharmaceuticals | Class I | Ongoing | 20240619 |
| D-1085-2023 | PLUVICTO 1,000MBq/mL (27 mCi/mL), lutetium Lu 177 vipivotide tetraxetan injection, 9.2 mL Single-dose vial, Manufacturer: Advanced Accelerator Appllications USA, Inc., 57 E. Willow Street NJ 07041, Milburn, USA, NDC 69488-010-61 | Advanced Accelerator Applications USA, Inc. | Class III | Terminated | 20230823 |
Frequently asked questions
What is Axe used for?
reduces underarm wetness
Who makes Axe?
Conopco, Inc. d/b/a Unilever is the labeler of record for Axe.
What form does Axe 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 Axe 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 Axe 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.