Quick answers
- What is After Bite?
- After Bite is a brand name of Sodium bicarbonate, Diphenhydramine, Camphor (synthetic), Lidocaine and Dimethicone, an over-the-counter medicine. The FDA NDC Directory lists 9 After Bite products in 8 strengths and forms.
- Who makes After Bite?
- Tender Corporation d/b/a Adventure Ready Brands lists 7 of the 9 After Bite products in the FDA NDC Directory.
- Is there a generic or store brand of After Bite?
- Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a After Bite product, 1 of them generic or store brands. Ask your pharmacist whether one is right for you.
- Has After Bite been recalled?
- No recall linked to After Bite products (by their NDC code or label) appears in the FDA enforcement reports we use.
What After Bite is
Each After Bite 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.
Sodium bicarbonate · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| sodium bicarbonate 0.7 g/14 g liquid (topical) | After Bite Advanced | None listed | — |
| sodium bicarbonate 1.04 g/20 g cream (topical) | After Bite Kids | 1 product, 1 company | DailyMed |
| sodium bicarbonate 50 mg/1000 mL liquid (topical) | After Bite X Tech | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Sodium bicarbonate →
Diphenhydramine · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| diphenhydramine hydrochloride 0.4 g/20 g gel (topical) | After Bite Outdoor, After Bite Xtra | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Diphenhydramine →
Camphor (synthetic) · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| camphor (synthetic) 0.0425 g/4.25 g salve (topical) | After Bite Natural | None listed | — |
| camphor (synthetic) 2.295 g/76.5 g solution (topical) | After Ivy Wipe | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Camphor (synthetic) →
Lidocaine · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| lidocaine hydrochloride anhydrous 1.425 g/57 g gel (topical) | After Burn | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Lidocaine →
Dimethicone · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| dimethicone 4 mg/mL cream (topical) | After Care | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Dimethicone →
FDA approval
After Bite 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 After Bite
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of After Bite products.
- Tender Corporation d/b/a Adventure Ready Brands7 products
- Adventure Ready Brands1 product
- Merz North America1 product
Recalls
No recall linked to After Bite 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.