NINJACOF COTTON CANDY FLAVOR- 16 OZ- antitussive and antihistamine liquid 
Eagle Labs Inc.

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Ninjacof Cotton Candy Flavor

Active Ingredient

Chlophedianol HCL

Pryilamine Maleate

Purpose

Anitussive

Antihistamine

USES

Temporarily relieves these symptoms due to the common cold, hayfever, (allergic rhinitis) or other upper respiratroy allergies.

Cough due to minor throat and bronchial irritation
Runny Nose
Sneezing
Itching of the Nose or Throat
Itchy, watery eyes

Warnings

Do not exceed recommended dosage.
DO NOT USE IF PRINTED SAFETY SEAL IS MISSING OR BROKEN.
Do not use this product
If you are now taking prescription monoamine oxidase inhibitor (MAOI) (certain
drugs for depression, psychiatric, or emotional conditions or Parkinsons disease),
or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription
drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if you have

A cough that lasts or is chronic such as occurs with smoking, asthma, or
emphysema.
A cough that occurs with too much phlegm (mucus)
Ask doctor or pharmacist before use if you are
Taking sedatives or tranquilizers
If you have a breathing problem such as emphysema or chronic bronchitis
If you have glaucoma
If you have difficulty in urination due to enlargement of the prostate gland

When using this product

Excitability may occur, especially in children.
Marked drowsiness may occur
Avoid alcoholic drinks
Alcohol, sedatives, and tranquilizers may increase drowsiness
Be careful when driving a motor vehicle or operating machinery

Stop use and ask a doctor if

Nervousness, dizziness, or sleeplessness occurs
Symptoms do not improve within 7 days or are
accompanied by a fever, rash, or persistent headache. A
persistent cough may be a sign of a serious condition.
New symptoms occur

Keep out of reach of children

In case of overdose, get medical help or contact a Poison
Control Center right away

Directions

Do not exceed recommended dosage.
In case of overdose, get medical help or contact a Poison
Control Center right away


Adults and children
12 years of age
and over: 2 teaspoonfuls (10mL) every 6 to 8
hours not to exceed 8 teaspoons in
24hr


Children 6 to under
12 years of age:1 teaspoonfuls (5ml) every 6 to 8
hours not to exceed 4 teaspoons in
24hr


Children under
6 years of age: Consult a doctor.

Other

Store at 20° - 25°C (68°- 77°F); excursions permitted to 15°-30°C
(59° - 86°F). [See USP Controlled Room Temperature].

Inactive Ingredients

Citric Acid, Glycerin, Natural & Artificial Flavors, Propylene Glycol,
Purified Water, Sodium Benzoate, Sodium Citrate, Sucralose

Questions? Comments?

To report a serious adverse event or obtain product
information, contact 1-866-959-4880

Ninjacof Cotton Candy Flavor 16 oz

Ninjacof 16oz

Ninjacof Cotton Candy Flavor 4 oz

Ninjacof 4oz

NINJACOF COTTON CANDY FLAVOR- 16 OZ 
antitussive and antihistamine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79804-032
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRILAMINE MALEATE (UNII: R35D29L3ZA) (PYRILAMINE - UNII:HPE317O9TL) PYRILAMINE MALEATE12.5 mg  in 5 mL
CHLOPHEDIANOL HYDROCHLORIDE (UNII: 69QQ58998Y) (CHLOPHEDIANOL - UNII:42C50P12AP) CHLOPHEDIANOL HYDROCHLORIDE12.5 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
SUCRALOSE (UNII: 96K6UQ3ZD4)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Product Characteristics
Color    Score    
ShapeSize
FlavorCOTTON CANDYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79804-032-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/17/2021
2NDC:79804-032-04118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/17/2021
3NDC:79804-032-0110 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/17/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01212/17/2021
Labeler - Eagle Labs Inc. (118496872)

Revised: 4/2024
Document Id: 16235cd7-a287-2c96-e063-6294a90a806b
Set id: a624be5f-c8b5-4105-bb87-4cd0c0e9edfb
Version: 4
Effective Time: 20240415
 
Eagle Labs Inc.