Verifying…
Home / Drug A–Z / Kescold Capsule

Kescold Capsule

NAFDAC Reg. No. 00-0000 · Drug

Registered with NAFDAC — registration activeAs of 5 November 2026 · synced automatically from official sources.
Product
Kescold Capsule
NAFDAC number
00-0000
Active ingredient
Chlorpheniramine Maleate; Phenylephrine Hydrochloride
Strength
4 mg; 2.5 mg
Form
Capsule
Pack size
10 x 10's
Manufacturer
Not listed
Applicant (holder)
Onifam Laboratories Limited
Approved
28 Sep 2021
Status
Inactive View on NAFDAC ↗
Registration valid to
27 Sep 2026
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • Kescold Capsule is on the NAFDAC register with an active registration (00-0000). 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. Not medical advice — always follow your doctor or pharmacist.

What Kescold Capsule is used for

From the official U.S. FDA label for chlorpheniramine maleate, the active ingredient registered with NAFDAC.

What it is used for

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: sneezing runny nose itchy, watery eyes itching of the nose or throat

Purpose

Antihistamine

Do not use if

to make a child sleepy.

Warnings

Do not use to make a child sleepy. Ask a doctor before use if you have glaucoma a breathing problem such as emphysema or chronic bronchitis difficulty in urination due to enlargement of the prostate gland Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers. When using this product drowsiness may occur avoid alcoholic beverages excitability may occur, especially in children use caution when driving a motor vehicle or operating machinery alcohol, sedatives, and tranquilizers may increase drowsiness If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. …

Pregnancy & breastfeeding

If pregnant or breast-feeding, ask a health professional before use.

Storage

store at 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF) protect from excessive moisture use by expiration date on package

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

Check your pack of Kescold Capsule

Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.

3 free checks left today · no signup Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Kescold Capsule

What is in Kescold Capsule?

Kescold Capsule contains Chlorpheniramine Maleate; Phenylephrine Hydrochloride (4 mg; 2.5 mg), as capsule, according to its NAFDAC registration record.

Is Kescold Capsule registered with NAFDAC?

Yes. Kescold Capsule is listed on the NAFDAC register under registration number 00-0000, and its registration is active as of 5 November 2026.

Has Kescold Capsule been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Kescold Capsule in our automatically synced alert list.

How can I check that my pack of Kescold Capsule is genuine?

Run a free authenticity scan with the NAFDAC number 00-0000, 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 Kescold Capsule used for?

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: sneezing runny nose itchy, watery eyes itching of the nose or throat (Summarised from the official U.S. FDA label for chlorpheniramine maleate. Always follow your doctor or pharmacist.)

Patient reviews

–No reviews yet
5★
0
4★
0
3★
0
2★
0
1★
0
Have you used Kescold Capsule? Share your experience to help other patients. Sign in to review

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