NEW HANBANG COL CAP- acetaminophen, caffeine anhydrous, tablet

New Hanbang Col Cap by

Drug Labeling and Warnings

New Hanbang Col Cap by is a Otc medication manufactured, distributed, or labeled by Lydia Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Acetaminophen, Caffeine Anhydrous,

PURPOSE

■ relieve your cold symptoms cold Rhinitis

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

INDICATIONS & USAGE

■ Adult and children 15 years of age and older: 2 capsules three times a day ■ Children under 15 years of age: ask a doctor

WARNINGS

■ When using this product Stop use and ask a doctor if nervousness, diziness, 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 symtoms occur. keep out of reach of children. In case of overdose, get medical help or contact a poison contral center right away. If pregnant or breast-feeding, ask a health professional before use.

INACTIVE INGREDIENT

magnesium stearate, corn, starch, etc

DOSAGE & ADMINISTRATION

for oral use

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NEW HANBANG COL CAP 
acetaminophen, caffeine anhydrous, tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72988-0032
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	150 mg
CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E)	CAFFEINE	12.5 mg

Inactive Ingredients
Ingredient Name	Strength
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	brown	Score	no score
Shape	OVAL	Size	20mm
Flavor		Imprint Code	JW
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72988-0032-1	12 in 1 PACKAGE; Type 0: Not a Combination Product	09/30/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/30/2022

Labeler - Lydia Co., Ltd. (695735569)

Registrant - Lydia Co., Ltd. (695735569)

Establishment
Name	Address	ID/FEI	Business Operations
Lydia Co., Ltd.		695735569	manufacture(72988-0032)