Quick answers
- What is Bactimicina Childrens?
- Bactimicina Childrens is a brand name of Camphor (synthetic), eucalyptus oil and menthol, Diphenhydramine, Chlorpheniramine and dextromethorphan, Acetaminophen and Dextromethorphan, guaifenesin and phenylephrine, an over-the-counter medicine. The FDA NDC Directory lists 5 Bactimicina Childrens products in 5 strengths and forms.
- Who makes Bactimicina Childrens?
- DLC Laboratories, Inc. lists 5 of the 5 Bactimicina Childrens products in the FDA NDC Directory.
- Is there a generic or store brand of Bactimicina Childrens?
- Yes. The FDA NDC Directory lists 106 other products with the same active ingredients, strength and form as a Bactimicina Childrens product, 106 of them generic or store brands. Ask your pharmacist whether one is right for you.
- Has Bactimicina Childrens been recalled?
- No recall linked to Bactimicina Childrens products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Bactimicina Childrens is
Each Bactimicina Childrens 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.
Camphor (synthetic), eucalyptus oil and menthol · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| camphor (synthetic) 4.8% · eucalyptus oil 1.2% · menthol 2.6% ointment (topical) | Bactimicina Vapor Rub | 25 products, 17 companies | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Camphor (synthetic), eucalyptus oil and menthol →
Diphenhydramine · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| diphenhydramine hydrochloride 12.5 mg/5 mL liquid (oral) | Bactimicina Childrens Allergy | 39 products, 29 companies | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Diphenhydramine →
Chlorpheniramine and dextromethorphan · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| chlorpheniramine maleate 1 mg/5 mL · dextromethorphan hydrobromide 7.5 mg/5 mL liquid (oral) | Bactimicina Childrens Cough and Cold | None listed | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Chlorpheniramine and dextromethorphan →
Acetaminophen · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| acetaminophen 160 mg/5 mL liquid (oral) | Bactimicina Childrens Pain and Fever | 41 products, 23 companies | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Acetaminophen →
Dextromethorphan, guaifenesin and phenylephrine · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| dextromethorphan hydrobromide 10 mg/5 mL · guaifenesin 100 mg/5 mL · phenylephrine hydrochloride 5 mg/5 mL solution (oral) | Bactimicina Cough and Cold | 1 product, 1 company | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Dextromethorphan, guaifenesin and phenylephrine →
FDA approval
Bactimicina Childrens 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 Bactimicina Childrens
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Bactimicina Childrens products.
- DLC Laboratories, Inc.5 products
Recalls
No recall linked to Bactimicina Childrens 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.