GANMAOLING- acetaminophen and chlorpheniramine maleate tablet

GANMAOLING by

Drug Labeling and Warnings

GANMAOLING by is a Otc medication manufactured, distributed, or labeled by ANHUI DONGSHENGYOUBANG PHARMACEUTICAL CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient (in each tablet)
Acetaminophen 60 mg
Chlorpheniramine maleate 0.667 mg

PURPOSE

Purpose
Pain reliever-fever reducer
Antihistamine

INDICATIONS & USAGE

Uses
Temporarily relieves the following symptoms associated with the common cold, hay fever, or other upper respiratory allergies:
minor aches and pains
headache
muscular aches
fever
sore throat
sneezing
itching of the nose or throat
runny nose
itchy, watery eyes

WARNINGS

Warnings

DO NOT USE

Do not use
for pain for more than 10 days
for fever for more than 3 days

ASK DOCTOR

Ask a doctor before use if the user has
glaucoma
a breathing problem such as emphysema or chronic bronchitis
difficulty in urination due to enlargement of the prostate gland

ASK DOCTOR/PHARMACIST

Ask a doctor or pharmacist before use if you are
taking sedatives or tranquilizers

WHEN USING

When using this product
may cause excitability especially in children
may cause drowsiness (alcohol, sedatives, and tranquilizers may increase the drowsiness effect)
avoid alcoholic beverages
use caution when driving a motor vehicle or operating machinery

STOP USE

Stop use and ask a doctor if
pain or fever persists or worsen
new symptoms occur
redness or swelling is present
sore throat:
     is severe
     last for more than 2 days
is accompanied or followed by:
     fever
     headache
     rash
     nausea
     vomiting

PREGNANCY OR BREAST FEEDING

If pregnant or breast-feeding, ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control
Center right away. Prompt medical attention is critical for adults as well as for children even if you do
not notice any signs or symptoms.

DOSAGE & ADMINISTRATION

Directions
adults and children 12 years of age and older: Take 6 tablets every 4 hours, not more than 36 tablets in 24 hours
children 6 to under 12 years of age: Take 3 tablets every 4 hours, not more than 18 tablets in 24 hours
children under 6 years: consult a doctor

STORAGE AND HANDLING

Other information
protect from light our excessive heat
keep tightly closed
keep in dry place

INACTIVE INGREDIENT

Inactive ingredients
Rough-leaved holly root, evodia root, wild chrysanthemum flower, Chinese chaste tree twig, honeysuckle flower, strobilanthes cusia root, cornstarch, sucrose, water, FD&C yellow no.5 and FD&C yellow no.6.

QUESTIONS

Questions or Comments? (888) 221-3496 M-F 9 am to 5 pm
you may also use this number to report serious adverse events associated with the use of this product

PRINCIPAL DISPLAY PANEL

GANMAOLING TABLETS, NDC: 72030-002-01, Antihistamine, Pain Reliever-Fever Reducer, 120 Tablets

INGREDIENTS AND APPEARANCE

GANMAOLING 
acetaminophen and chlorpheniramine maleate tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72030-002
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	60 mg
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U)	CHLORPHENIRAMINE MALEATE	0.667 mg

Inactive Ingredients
Ingredient Name	Strength
ILEX ASPRELLA ROOT (UNII: S7K9P1V8VG)
MELICOPE PTELEIFOLIA ROOT (UNII: Z400593S4G)
CHRYSANTHEMUM INDICUM FLOWER (UNII: I6OER6U04L)
VITEX NEGUNDO WHOLE (UNII: C92PGK11XB)
LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
STROBILANTHES CUSIA ROOT (UNII: F1919HP06B)
STARCH, CORN (UNII: O8232NY3SJ)
SUCROSE (UNII: C151H8M554)
WATER (UNII: 059QF0KO0R)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)

Product Characteristics
Color	yellow	Score	no score
Shape	ROUND	Size	10mm
Flavor		Imprint Code	GM
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72030-002-01	1 in 1 BOX	11/26/2018
1		120 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	11/26/2018

Labeler - ANHUI DONGSHENGYOUBANG PHARMACEUTICAL CO., LTD. (527929527)

Establishment
Name	Address	ID/FEI	Business Operations
ANHUI DONGSHENGYOUBANG PHARMACEUTICAL CO., LTD.		527929527	manufacture(72030-002)