PROHIBIT SOLUBLE DRENCH POWDER- levamisole hydrochloride powder, for solution 
Huvepharma, Inc

----------

PROHIBIT®
(levamisole hydrochloride)
Soluble Drench Powder

NDC 23243-2320-5
PROHIBIT®
(levamisole hydrochloride)
Soluble Drench Powder
Anthelmintic
Each packet contains 46.8 grams of levamisole hydrochloride activity.

CATTLE AND SHEEP DEWORMER FOR ORAL USE
Administer as a standard drench with standard drench syringe or administer as a concentrated
drench solution with an automatic drenching syringe.

INDICATIONS:
Prohibit (levamisole hydrochloride) is a broad-spectrum anthelmintic and is effective against
the following nematode infections in cattle and sheep:

SHEEP:
STOMACH WORMS: Haemonchus contortus, Trichostrongylus axei, Teladorsagia circumcincta.
INTESTINAL WORMS: Trichostrongylus colubriformis, Cooperia curticei, Nematodirus spathiger,
Bunostomum trigonocephalum, Oesophagostomum columbianum, Chabertia ovina.
LUNGWORMS: Dictyocaulus filaria.

CATTLE:
STOMACH WORMS: Haemonchus placei, Trichostrongylus axei, Ostertagia ostertagi.
INTESTINAL WORMS: Trichostrongylus longlspicularis, Cooperia oncophora, Cooperia punctata,
Nematodirus spathiger, Bunostomum phiebotomum, Oesophagostomum radiatum.
LUNGWORMS: Dictyocaulus viviparus.

NOT FOR USE IN HUMANS
KEEP OUT OF REACH OF CHILDREN
Restricted Drug (California) Use Only as Directed
Approved by FDA under ANADA # 200-225

NET WEIGHT: 1.8 oz (52 g)

HUVEPHARMA®

Manufactured for Huvepharma, Inc.
Peachtree City, GA 30269
®Registered Trademark of Huvepharma, Inc.

DOSAGE AND ADMINISTRATION

 CATTLE–STANDARD DRENCH SOLUTION: Place the contents of this  packet in a 1 quart (32 fl. oz.) container, fill with water, swirl until dissolved. Administer as a single drench dose according to the following table:

 SHEEP–STANDARD DRENCH SOLUTION: Place the contents of this  packet in a 1 gallon (128 fl. oz.) container, fill with water, swirl until dissolved. Administer as a single drench dose according to the following table:

 Weight

Drench dosage

Packet Will Treat

 Weight

Drench Dosage

Packet Will Treat

 200 lb.

1/2 fl. oz.

64 head

 50 lb.

1/2 fl. oz.

256 head

 400 lb.

1 fl. oz.

32 head

 100 lb.

1 fl. oz.

128 head

 650 lb.

1 1/2 fl. oz.

21 head

 150 lb.

1 1/2 fl. oz.

84 head

 800 lb.

2 fl. oz.

16 head

 200 lb.

2 fl. oz.

64 head

 CONCENTRATED DRENCH SOLUTION: For use with automatic syringe.   Place the contents of this packet in a standard household measuring container   and add water to the 8 3/4 fl. oz. level; or use the measuring container   available from your supplier and add water to the mark. Swirl until dissolved.   Give 2 ml (milliliter) per 100 lb. body weight. Refer to the table above for the   number of cattle this packet will treat.

 CONCENTRATED DRENCH SOLUTION: For use with   automatic syringe. Place the contents of this packet in a   standard household measuring container and add water to the   17 1/2 fl. oz. level. Swirl until dissolved. Give 2 ml per 50 lb.   body weight. Refer to the table above for the number of sheep   this packet will treat.

Do not underdose. Ensure each animal receives a complete dose based on a current body weight.
Underdosing may result in ineffective treatment, and encourage the development of parasite resistance.

NOTE: Careful weight estimates are essential for proper performance of this product. Prepare solutions
as needed. However, excess solutions may be stored in clean closed containers up to 90 days without
loss of anthelmintic activity. Cattle and Sheep maintained under conditions of constant helminth
exposure may require re-treatment within two to four weeks after the first treatment.

RESIDUE WARNING: Do not administer to cattle within 48 hours of slaughter for food. Do
not administer to sheep within 72 hours of slaughter for food. To prevent residues in milk,
do not administer to dairy animals of breeding age.

OTHER WARNINGS: Parasite resistance may develop to any dewormer, and has been
reported for most classes of dewormers. Treatment with a dewormer used in
conjunction with parasite management practices appropriate to the geographic
area and the animal(s) to be treated may slow the development of parasite
resistance. Fecal examinations or other diagnostic tests and parasite
management history should be used to determine if the product is appropriate
for the herd/flock, prior to the use of any dewormer. Following the use of any
dewormer, effectiveness of treatment should be monitored (for example, with
the use of a fecal egg count reduction test or another appropriate method).
A decrease in a drug's effectiveness over time as calculated by fecal egg
count reduction tests may indicate the development of resistance to the
dewormer administered. Your parasite management plan should be adjusted
accordingly based on regular monitoring.

CAUTION: Muzzle foam may be observed. However, this reaction will
disappear within a few hours. If this condition persists, a veterinarian
should be consulted. Follow recommended dosage carefully. Consult
veterinarian before using in severely debilitated animals.
Consult your veterinarian for assistance in the diagnosis, treatment,
and control of parasitism.

To report suspected adverse drug events, for technical assistance or to
obtain a copy of the Safety Data Sheet (SDS), contact Huvepharma, Inc.
at 1-877-994-4883 or www.huvepharma.us. For additional information about
adverse drug experience reporting for animal drugs, contact FDA at
1-888-FDA-VETS or http://www.fda.gov/reportanimalae.

Store between 20–25ºC (68-77ºF).    MF: L-6232-05    Rev: 03-2022
HOW SUPPLIED: 52 g (1.8 oz) and 605 g (21.34 oz)

LOT                      EXP.

Take Time

NDC 23243-2320-6
PROHIBIT®
(levamisole hydrochloride)
Soluble Drench Powder
Anthelmintic

CATTLE AND SHEEP DEWORMER
FOR ORAL USE
This bottle contains 544.5 grams of
levamisole hydrochloride activity.

Not For Use in Humans

Keep Out of Reach of Children

Restricted Drug (California) -
Use Only as Directed

Approved by FDA under ANADA # 200-225

Net Wt: 21.34 oz (1.3 lb.) (605 g)

INDICATIONS: PROHIBIT (levamisole hydrochloride) is a broad-spectrum anthelmintic and is
effective against the following nematode infections in cattle and sheep:
SHEEP:
STOMACH WORMS: Haemonchus contortus, Trichostrongylus axei, Teladorsagia circumcincta.
INTESTINAL WORMS: Trichostrongylus colubriformis, Cooperia curticei, Nematodirus spathiger,
Bunostomum trigonocephalum, Oesophagostomum columbianum, Chabertia ovina.
LUNGWORMS: Dictyocaulus filaria.
CATTLE:
STOMACH WORMS: Haemonchus placei, Trichostrongylus axei, Ostertagia ostertagi.
INTESTINAL WORMS: Trichostrongylus longlspicularis, Cooperia oncophora, Cooperia punctata,
Nematodirus spathiger, Bunostomum phiebotomum, Oesophagostomum radiatum.
LUNGWORMS: Dictyocaulus viviparus.

RESIDUE WARNING: Do not administer to cattle within 48 hours of slaughter
for food. Do not administer to sheep within 72 hours of slaughter for food. To
prevent residues in milk, do not administer to dairy animals of breeding age.

OTHER WARNINGS: Parasite resistance may develop to any dewormer, and has been reported
for most classes of dewormers. Treatment with a dewormer used in conjunction with parasite
management practices appropriate to the geographic area and the animal(s) to be treated may
slow the development of parasite resistance. Fecal examinations or other diagnostic tests and
parasite management history should be used to determine if the product is appropriate for the
herd/flock, prior to the use of any dewormer. Following the use of any dewormer, effectiveness
of treatment should be monitored (for example, with the use of a fecal egg count reduction
test or another appropriate method). A decrease in a drug's effectiveness over time as
calculated by fecal egg count reduction tests may indicate the development of resistance to
the dewormer administered. Your parasite management plan should be adjusted accordingly
based on regular monitoring.

CAUTION: Muzzle foam may be observed. However, this reaction will disappear within a few
hours. If this condition persists, a veterinarian should be consulted. Follow recommended
dosage carefully. Consult veterinarian before using in severely debilitated animals.

Consult your veterinarian for assistance in the diagnosis, treatment, and control of parasitism.

Store between 20º-25ºC (68º-77ºF).

HOW SUPPLIED: 52 g (1.8 oz) and 605 g (21.34 oz)

®Registered trademark of Huvepharma, Inc.
Manufactured for
Huvepharma, Inc.
Peachtree City, GA 30269

MF# L-6232-60

Rev. 03-2022

LOT.:                  EXP. DATE

Take Time

DOSAGE AND ADMINISTRATION: When you are ready to deworm your cattle or sheep, add water to the powder in this bottle up to the 3 liter mark. Swirl to mix thoroughly before using. If any solution is left over, it may be stored for up to 3 months in this tightly capped bottle, shake well before using.

DATE WATER WAS ADDED TO THIS BOTTLE

                                                Month       Day       Year

Administer as a single drench dose as follows:

CATTLE--2 mL per 100 lb. body weight

Weight

Drench dosage

Bottle

Will Treat

100 lb.

2 mL

1,500 head

300 lb.

6 mL

500 head

500 lb.

10 mL

300 head

700 lb.

14 mL

214 head

1,000 lb.

20 mL

150 head

SHEEP--1 mL per 50 lb. body weight

Weight

Drench dosage

Bottle

Will Treat

50 lb.

1 mL

3,000 head

100 lb.

2 mL

1,500 head

150 lb.

3 mL

1,000 head

200 lb.

4 mL

750 head

Do not underdose. Ensure each animal receives a complete dose based on a current body weight.
Underdosing may result in ineffective treatment, and encourage the development of parasite resistance.

NOTE: Careful weight estimates are essential for proper performance of this
product. Cattle and sheep maintained under conditions of constant helminth
exposure may require retreatment within two to four weeks after the first
treatment.

To report suspected adverse drug events, for technical assistance or to
obtain a copy of the Safety Data Sheet (SDS), contact Huvepharma, Inc. at
1-877-994-4883 or www.huvepharma.us. For additional information about
adverse drug experience reporting for animal drugs, contact FDA at
1-888-FDA-VETS or http://www.fda.gov/reportanimalae.

Packet Label Front

Packet Label Back

HVP_Prohibit_605 g_03-2022

PROHIBIT  SOLUBLE DRENCH POWDER
levamisole hydrochloride powder, for solution
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:23243-2320
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LEVAMISOLE HYDROCHLORIDE (UNII: DL9055K809) (LEVAMISOLE - UNII:2880D3468G) LEVAMISOLE0.9 g  in 1 g
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:23243-2320-552 g in 1 PACKET
2NDC:23243-2320-6605 g in 1 JUG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANADAANADA20022504/20/2022
Labeler - Huvepharma, Inc (619153559)
Registrant - Huvepharma EOOD (552671651)

Revised: 12/2023
Document Id: e24cd6cc-0864-4d87-ad56-02359b1ad205
Set id: baf0da35-573e-4abb-bdef-18870d5f5f72
Version: 2
Effective Time: 20231218
 
Huvepharma, Inc