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Uch-Ject Syringe with Needle (2 mL,5 mL,10 mL, 20 mL)

NAFDAC Reg. No. 03-6213 · Drug

Registered with NAFDAC. Registration activeAs of 27 October 2026 · synced automatically from official sources.
Product
Uch-Ject Syringe with Needle (2 mL,5 mL,10 mL, 20 mL)
NAFDAC number
03-6213
Active ingredient
Syringes and Needles
Strength
NA
Form
NA
Pack size
100 x 2 mL; 100 x 5 mL; 100 x 10 mL; 80 x 20 mL packs
Manufacturer
Not listed
Applicant (holder)
Crystal-Uch Nigeria Ltd
Approved
1 Nov 2022
Status
Active View on NAFDAC ↗
Registration valid to
26 Oct 2027
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Uch-Ject Syringe with Needle (2 mL,5 mL,10 mL, 20 mL) is on the NAFDAC register with an active registration (03-6213). 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.

What Uch-Ject Syringe with Needle (2 mL,5 mL,10 mL, 20 mL) is used for

From the official U.S. FDA label for Uch-Ject Syringe with Needle (2 mL,5 mL,10 mL, 20 mL), the active ingredient registered with NAFDAC.

What it is used for

For the temporary relief of allergy and hay fever symptoms including: Sneezing Runny Nose Itchy Eyes, Nose, Throat

Purpose

Urtica Dioica Certified Organic 8C Treats Hives or Other Rash-Like Eruptions Althaea Officinalis 34C For Itching, Rash Like Symptoms Inula Helenium 55C Expectorant, for Respiratory Issues Angelica Arc …

Possible side effects

Stop use and ask doctor if symptoms persist for more than 3 days or worsen. When using this product, rinse right away with water if it gets in the eyes.

Warnings

For oral (sublingual) use. Ask a doctor before use in children under 3 years of age. Stop use and ask doctor if symptoms persist for more than 3 days or worsen. When using this product, rinse right away with water if it gets in the eyes. If pregnant or breast-feeding ask a doctor before use. Keep out of reach of children.

Pregnancy & breastfeeding

If pregnant or breast-feeding ask a doctor before use.

Storage

Store in a cool, dark place Store upright Tighten cap after use to prevent oxidation

General information only, not dosing advice. Always follow the leaflet in your pack and your doctor or pharmacist.

NAFDAC recall & alert notices

Regulatory Clarification on Deleject Disposable Needle Public Alert13 Aug 2026 · nafdac.gov.ngThe public Alert No. 042/2026, concerning the reported presence of whitish particulate matter in Deleject Disposable Needle Batch No. 240605, was uploaded onto the NAFDAC website in error.The matter had earlier undergone appropriate regulatory review and investigation and was satisfactorily resolved several months ago.…Public Alert No.44/2025 – Recall of Mivacron Injection 0.2%, Nimbex Injection 2mg/ml Over Safety Concerns19 Dec 2025 · nafdac.gov.ngThe National Agency for Food and Drug Administration and Control (NAFDAC) received an intelligence report from the Office of the Secretary to the Government of the Federation (OSGF) about the recall of Mivacron injection 0.2% and Nimbex injection 2mg/ml by Hong Kong Department of Health due to safety concerns.The Hong …Public Alert No. 031/2025 – Alert on the Presence of an Unauthorized/ Unregistered Darzalex (Daratumumab) 1800mg/15ml vial SC Injection in Nigeria 15 Oct 2025 · nafdac.gov.ngThe National Agency for Food and Drugs Administration and Control (NAFDAC) is alerting the public on the sale of an unauthorized and unregistered brand of Daratumumab formulation in Nigeria.An internal investigation conducted by Johnson & Johnson revealed that there are two different packaging designs for their Daratum…Public Alert No. 028/2025 – Alert on Unregistered/Falsified Oxytocin Injection  25 Aug 2025 · nafdac.gov.ngThe National Agency for Food and Drug Administration and Control (NAFDAC) hereby alerts the public about an unregistered Gold Vision Oxytocin injection 10IU with a fake NAFDAC Reg. No. A4-9566. The product is purportedly manufactured by Anhui Hongye Pharmaceutical Co., Ltd., Fengyang East Road, Bengbu, Anhui Province, …

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

Check your pack of Uch-Ject Syringe with Needle (2 mL,5 mL,10 mL, 20 mL)

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

3 free checks left today Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Uch-Ject Syringe with Needle (2 mL,5 mL,10 mL, 20 mL)

What is in Uch-Ject Syringe with Needle (2 mL,5 mL,10 mL, 20 mL)?

Uch-Ject Syringe with Needle (2 mL,5 mL,10 mL, 20 mL) contains Syringes and Needles (NA), as na, according to its NAFDAC registration record.

Is Uch-Ject Syringe with Needle (2 mL,5 mL,10 mL, 20 mL) registered with NAFDAC?

Yes. Uch-Ject Syringe with Needle (2 mL,5 mL,10 mL, 20 mL) is listed on the NAFDAC register under registration number 03-6213, and its registration is active as of 27 October 2026.

Has Uch-Ject Syringe with Needle (2 mL,5 mL,10 mL, 20 mL) been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Uch-Ject Syringe with Needle (2 mL,5 mL,10 mL, 20 mL) in our automatically synced alert list.

How can I check that my pack of Uch-Ject Syringe with Needle (2 mL,5 mL,10 mL, 20 mL) is genuine?

Run a free authenticity scan with the NAFDAC number 03-6213, 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.

What is Uch-Ject Syringe with Needle (2 mL,5 mL,10 mL, 20 mL) used for?

For the temporary relief of allergy and hay fever symptoms including: Sneezing Runny Nose Itchy Eyes, Nose, Throat (Summarised from the official U.S. FDA label for Uch-Ject Syringe with Needle (2 mL,5 mL,10 mL, 20 mL). 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.