Quick answers
- What is Zims Max Freeze?
- Zims Max Freeze is a brand name of Menthol, Lidocaine and menthol, Camphor (synthetic) and menthol, unspecified form and Camphor (synthetic), menthol, unspecified form and methyl salicylate, an over-the-counter medicine. The FDA NDC Directory lists 7 Zims Max Freeze products in 6 strengths and forms.
- Who makes Zims Max Freeze?
- KOBAYASHI Healthcare International, Inc. lists 7 of the 7 Zims Max Freeze products in the FDA NDC Directory.
- Is there a generic or store brand of Zims Max Freeze?
- Yes. The FDA NDC Directory lists 6 other products with the same active ingredients, strength and form as a Zims Max Freeze product, 6 of them generic or store brands. Ask your pharmacist whether one is right for you.
- Has Zims Max Freeze been recalled?
- No recall linked to Zims Max Freeze products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Zims Max Freeze is
Each Zims Max Freeze product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Menthol · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| menthol, unspecified form 16% spray (topical) | Zims Max Freeze Pro Formula | 1 product, 1 company | DailyMed |
| menthol, unspecified form 160 mg/mL liquid (topical) | Zims Max Freeze Pro Formula | 4 products, 4 companies | DailyMed |
| menthol, unspecified form 7% gel (topical) | Zims Max Freeze Pro Formula | 1 product, 1 company | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Menthol →
Lidocaine and menthol · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| lidocaine hydrochloride 760 mg · menthol, unspecified form 190 mg patch (topical) | Zims Max Freeze | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Lidocaine and menthol →
Camphor (synthetic) and menthol, unspecified form · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| camphor (synthetic) 950 mg · menthol, unspecified form 950 mg patch (topical) | Zims Max Freeze Leg Cramps | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Camphor (synthetic) and menthol, unspecified form →
Camphor (synthetic), menthol, unspecified form and methyl salicylate · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| camphor (synthetic) 31 mg/mL · menthol, unspecified form 50 mg/mL · methyl salicylate 115 mg/mL liquid (topical) | Zims Max Freeze Leg Cramp | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Camphor (synthetic), menthol, unspecified form and methyl salicylate →
FDA approval
Zims Max Freeze products are sold under an FDA over-the-counter monograph: rules that set the allowed active ingredients, strengths and label wording, so these products do not need an individual FDA approval.
Companies that list Zims Max Freeze
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Zims Max Freeze products.
- KOBAYASHI Healthcare International, Inc.7 products
Recalls
No recall linked to Zims Max Freeze products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.