Label: PRO-CHLO- chlophedianol hydrochloride, phenylephrine hydrochloride, pyrilamine maleate liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 66594-321-01, 66594-321-16 - Packager: Pro-Pharma, LLC
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated November 16, 2011
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Uses
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Warnings
Do not exceed recommended dosage.
Do not use this product
- if you are now taking a prescription monoamine oxidase inhibibor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's 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)
- heart disease
- high blood pressure
- thyroid disease
- diabetes
- trouble urinating due to an enlarged prostate gland
- a breathing problem such as emphysema or chronic bronchitis
- glaucoma
When using this product
- excitability may occur, especially in children
- may cause marked drowsiness
- avoid alcoholic drinks
- alcohol, sedatives, and tranquilizers may increase the drowsiness effect
- be careful when driving a motor vehicle or operating machinery
- if you are now taking a prescription monoamine oxidase inhibibor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's 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.
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Directions
Do not exceed recommended dosage.
Adults and
children 12
years of age
and over:
2 teaspoonfuls (10 mL)
every 6 hours, not to
exceed 8 teaspoonfuls in
24 hours
Children 6 to
under 12 years
of age:
1 teaspoonful (5 mL)
every 6 hours, not to
exceed 4 teaspoonfuls in
24 hours
Children under
6 years of age:
Consult a doctor.
- Other information
- Inactive ingredients
- Questions? Comments?
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Product Packaging
The packaging below represents the labeling currently used:
Principal display panel and side panel for 473 mL label:
NDC #66594-321-16
PRO-CHLO
LIQUID
ALCOHOL FREE·GLUTEN FREE·SUGAR FREE
ANTITUSSIVE · NASAL DECONGESTANT
· ANTIHISTAMINE
Each teaspoonful (5 mL) contains:
CHLOPHEDIANOL HCL...............................12.5 mg
PHENYLEPHRINE HCL....................................5 mg
PYRILAMINE MALEATE..............................12.5 mg
Cotton Candy Flavor
PATENT PENDING
16 FL. OZ. (473 mL)
PRO-PHARMA LLC
Tamper evident by foil seal under cap. Do not use if foil
seal is broken or missing.
Dispense in a tight, light-resistant container with a child-resistant
cap.
THIS BOTTLE IS NOT TO BE DISPENSED TO THE CONSUMER.
Patent Pending
Manufactured by:
Great Southern Laboratories,
Houstin, TX 77099
Distributed for:
Pro-Pharma, LLC
Kirksville, MO 63501
Iss. 10/11
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INGREDIENTS AND APPEARANCE
PRO-CHLO
chlophedianol hydrochloride, phenylephrine hydrochloride, pyrilamine maleate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66594-321 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Chlophedianol Hydrochloride (UNII: 69QQ58998Y) (Chlophedianol - UNII:42C50P12AP) Chlophedianol Hydrochloride 12.5 mg in 5 mL Phenylephrine Hydrochloride (UNII: 04JA59TNSJ) (Phenylephrine - UNII:1WS297W6MV) Phenylephrine Hydrochloride 5 mg in 5 mL Pyrilamine Maleate (UNII: R35D29L3ZA) (Pyrilamine - UNII:HPE317O9TL) Pyrilamine Maleate 12.5 mg in 5 mL Inactive Ingredients Ingredient Name Strength Citric Acid Monohydrate (UNII: 2968PHW8QP) Glycerin (UNII: PDC6A3C0OX) Propylene Glycol (UNII: 6DC9Q167V3) Water (UNII: 059QF0KO0R) Sodium Citrate (UNII: 1Q73Q2JULR) Saccharin Sodium (UNII: SB8ZUX40TY) Sorbitol (UNII: 506T60A25R) Product Characteristics Color Score Shape Size Flavor COTTON CANDY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66594-321-16 473 mL in 1 BOTTLE 2 NDC:66594-321-01 30 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 12/12/2011 Labeler - Pro-Pharma, LLC (781088146) Registrant - Great Southern Laboratories (056139553) Establishment Name Address ID/FEI Business Operations Great Southern Laboratories 056139553 manufacture