NOCOLD-F- acetaminophene. chlorpheniramine maleate, dextromethorphan hydrobromide liquid

NOCOLD-F by

Drug Labeling and Warnings

NOCOLD-F by is a Otc medication manufactured, distributed, or labeled by Lydia Co., Ltd. , Lydia Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACETAMINOPHENE. CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMID

PURPOSE

First symtoms of a cold(snot, nasal stuffiness, sneeze, throat pain, cough, phlegm, chill, pyrexia, headache, arthralgia, myalgia) alleviate

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

INDICATIONS & USAGE

adult and children 16 years and over: take 1 bottle per session 3 times a day after meal

children 11 to 15 years: take 2/3 bottle once a day

children 7 to 10 years: take 1/2 bottle once a day

children 3 to 6 years: take 1/3 bottle once a day

children 2 years: take 1/4 bottle once a day

under 2 years: ask a doctor

WARNINGS

When using this product
Do not use for a period longer than 1 weeks
Stop use and ask a doctor if nervousness, dizziness, or sleepness occur. Pain, nasal congestion or cough gets worse or lasts more than 7 days.
fever gets worse or lasts more than 3 days
New symptoms occur
These may be signs of a serious condition.
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children, In case of overdose, get medical help or contact a poison control center right away

INACTIVE INGREDIENT

SODIUM BENZOATE, CITRIC ACID MONOHYDRATE,
SODIUM CITRATE DIHYDRATE, L-SODIUM GLUTAMATE, SUGAR,
D-SORBITOL SOLUTION, DISTILLED WATER

DOSAGE & ADMINISTRATION

For oral use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NOCOLD-F 
acetaminophene. chlorpheniramine maleate, dextromethorphan hydrobromide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72988-0027
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	200 mg  in 30 mL
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	15 mg  in 30 mL
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U)	CHLORPHENIRAMINE MALEATE	2.5 mg  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72988-0027-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/14/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/14/2021

Labeler - Lydia Co., Ltd. (695735569)

Registrant - Lydia Co., Ltd. (695735569)

Establishment
Name	Address	ID/FEI	Business Operations
Lydia Co., Ltd.		695735569	manufacture(72988-0027) , label(72988-0027)