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SII Td-Vac Vaccine

NAFDAC Reg. No. A6-100195 · Drug

Registered with NAFDAC. Registration activeAs of 3 November 2026 · synced automatically from official sources.
Product
SII Td-Vac Vaccine
رقم NAFDAC
A6-100195
المادة الفعالة
Tetanus Toxoid; Diphtheria Toxoid
التركيز
0.5 mL
الشكل
Suspension for injection
حجم العبوة
0.5 mL x 5 x 10's (in ampoules)
Manufacturer
Not listed
Applicant (holder)
Emzor Pharmaceutical Industries Limited
Approved
30 Apr 2025
الحالة
Active View on NAFDAC ↗
التسجيل ساري حتى
29 Apr 2030
تنبيهات منظمة الصحة العالمية
None found
Community reports
None
Times checked
0

About the medicine: Tetanus toxoid: uses, dosage and brands worldwide

What we found

  • SII Td-Vac Vaccine is on the NAFDAC register with an active registration (A6-100195). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

How to use SII Td-Vac Vaccine

ما تقوله النشرة الرسمية. إذا وصفه لك طبيب، فاتبع الوصفة. وإذا اختلفت نشرة عبوتك، فالأولوية لها.

لمن هو

• For the temporary relief of symptoms including: • cough • fever • congestion These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

كيف يُتناول وكم مرة
  • 1-10 drops under the tongue, 3 times a day or as directed by a health professional
  • Consult a physician for use in children under 12 years of age
Warnings

If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.

How to store it

Keep out of reach of children.

إذا نسيت جرعة

تناولها عندما تتذكر، إلا إذا اقترب موعد الجرعة التالية. عندها تخطَّ الجرعة المنسية. لا تتناول جرعتين معًا أبدًا للتعويض. راجع النشرة، فبعض الأدوية مختلفة.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2024-02-19.

Label for tetanus toxoid and diphtheria toxoid, the active ingredient registered with NAFDAC.

NAFDAC recall & alert notices

Public Alert No. 027/2023 – Alert on Fake Anthrax Vaccine Discovered in Some States in Nigeria1 Sep 2023 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC) is notifying the public of the discovery of fake anthrax vaccines circulating in Nasawara, Kaduna, Kwara and Oyo States. Following the current outbreak of anthrax in the country, the fake vaccines were discovered to be sold at major livestock m…Important Covid-19 Vaccine Safety Communication To Healthcare Providers27 May 2021 · nafdac.gov.ng, Important Covid-19 Vaccine Safety Communication To Healthcare Providers KEY POINTS    Possible Rare Event, Severe Allergic Reactions (Anaphylaxis) and Thromboembolic Events with Some Covid-19 Vaccines (probably due to underlying medical conditions and use of certain medications). Possible contraindications with Non…Public Alert No. 0008/2019 – Alert on Falsified Mencevax Meningitis Vaccines Circulating in Niger Republic15 Apr 2019 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC) alerts the public, especially the health care providers on the circulation of falsified MencevaxTM ACWY vaccines in Niger Republic. The Health Authorities of Niger Republic issued an alert on the falsified vaccines discovered during routine in…Public Alert No. 0006/2019 – Alert on Falsified Dukoral Oral Cholera Vaccines Circulating in Bangladesh26 Mar 2019 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC) alerts the public, especially the health care providers on the circulation of falsified Dukoral Oral Cholera vaccine circulating in Bangladesh. The packaging of the falsified Dukoral vaccine displays text in English and French language. The Wo…

Compare the brands and batch numbers in these notices with your pack, or enter your batch number above.

Check your pack of SII Td-Vac Vaccine

Add the expiry date on your pack for a full Trust Score.

أو التقط صورًا للعبوة
تبقّت 3 عمليات تحقق مجانية اليوم Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About SII Td-Vac Vaccine

What is in SII Td-Vac Vaccine?

SII Td-Vac Vaccine contains Tetanus Toxoid; Diphtheria Toxoid (0.5 mL), as suspension for injection, according to its NAFDAC registration record.

Is SII Td-Vac Vaccine registered with NAFDAC?

Yes. SII Td-Vac Vaccine is listed on the NAFDAC register under registration number A6-100195, and its registration is active as of 3 November 2026.

Has SII Td-Vac Vaccine been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches SII Td-Vac Vaccine in our automatically synced alert list.

How can I check that my pack of SII Td-Vac Vaccine is genuine?

Run a free authenticity scan with the NAFDAC number A6-100195, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

How do I take SII Td-Vac Vaccine?

Follow your prescription or the leaflet in your pack. The official label says: 1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.…

What is SII Td-Vac Vaccine used for?

• For the temporary relief of symptoms including: • cough • fever • congestion These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. (Summarised from the official U.S. FDA label for tetanus toxoid and diphtheria toxoid. Always follow your doctor or pharmacist.)

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Reviews are personal experiences from PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.