DEWORMER FOR DOG- pyrantel pamoate suspension

DEWORMER FOR DOG by

Drug Labeling and Warnings

DEWORMER FOR DOG by is a Otc medication manufactured, distributed, or labeled by Shenzhen Zhenshangzekai Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Pyrantel Pamoate

ASK DOCTOR

The presence of these parasites should be confirmed by laboratory fecal exam.
Dogs maintained under conditions of constant exposure to worm infestation should have a follow-up fecal exam within 2-4 weeks after treatment.
Consult your veterinarian for assistance in the diagnosis, treatment, and control of parasitism.

DO NOT USE

NOT FOR USE IN HUMANS

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

PURPOSE

dewormer

WHEN USING

Puppies: Treat at 2, 3, 4, 6, 8, and 10 weeks of age.

Lactating Bitches: Treat 2-3 weeks after whelping.

Adult Dogs: Dogs kept in heavily contaminated quarters may be treated at monthly intervals to prevent T. canis reinfestation.

DOSAGE & ADMINISTRATION

DEWORMER FOR DOG

suspension

INDICATIONS & USAGE

For the removal of large roundworms(Toxocara canis and Toxascaris leonina)and hookworms (Ancylostoma caninumand Uncinaria stenocephala) in dogsand puppies.

INACTIVE INGREDIENT

Water

INACTIVE INGREDIENT

Purified Water, Natural Flavor, Xanthan Gum, Citric Acid, Potassium Sorbate

INDICATIONS & USAGE

For the removal of large roundworms(Toxocara canis and Toxascaris leonina)and hookworms (Ancylostoma caninumand Uncinaria stenocephala) in dogsand puppies.

WARNINGS

ANIMAL SAFETY: Keep this product in asecure location out of reach of dogs,cats, and other animals to preventaccidental ingestion or overdose.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DEWORMER FOR DOG 
pyrantel pamoate suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87276-262
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRANTEL PAMOATE (UNII: 81BK194Z5M) (PYRANTEL - UNII:4QIH0N49E7)	PYRANTEL	4.54 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CITRIC ACID (UNII: 2968PHW8QP)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87276-262-01	1 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M024	03/01/2026

Labeler - Shenzhen Zhenshangzekai Technology Co., Ltd. (518601007)