Description
New Lulu A Tablet S is the basic medicine in the new LULU series. It contains the basic ingredients to relieve the symptoms of common cold (cough, nasal discharge, fever) and is the oldest and most commonly used medicine in Japanese homes.It combines 9 ingredients and is effective for 11 types of cold symptoms. It also contains the expectorant ingredient bromhexine hydrochloride, along with the long-lasting antihistamine ingredient for runny nose: clomidine fumarate, and the parasympathetic blocking ingredient: total suberine alkaloids.
It is a non-bitter sugar-coated tablet designed to be taken even by people who are not good at swallowing medications.
Specification
Place of manufacture (manufacturer): Japan (Daiichi Sankyo Company)
Quantity: 150 capsules
Efficacy
Relieves various symptoms of colds (runny nose, nasal congestion, sneezing, sore throat, cough, phlegm, chills, fever, etc.) (︑Headache︑Joint pain︑Muscle pain)
Dosage
Please take the following with cold or hot water. Take 3 times a day, within 30 minutes after meals.
Adults (15 years old and above): 3 tablets/time12 years old - under 15 years old: 2 tablets/timeUnder 12 years old: Do not take
Usage and dosage precautions
(1) Strictly observe the usage and dosage.(2) Children over 12 years of age should be supervised by a parent when taking this product.
Ingredient Dosage (Content as per 9 tablets)
- Acetaminophen･････････････ 900 mg
- Clemastine fumarate･････････････ 1.34 mg
- Dihydrocodeine phosphate･････････････ 24 mg
- Noscapine･････････････ 48 mg
- dl-methylephedrine hydrochloride･････････････ 60 mg
- Guaiacol sulfonic acid potassium･････････････ 240 mg
- Anhydrous caffeine･････････････ 75 mg
- Benfotiamine (vitamin B1 derivative)･････････････ 24 mg2. Additives: Cellulose, magnesium aluminometasilicate, CMC-Ca, hydroxypropyl cellulose, magnesium stearate, gum arabic, titanium oxide, stearic acid, refined sugar, talc, hypromellose, polyvinyl acetal diethyl aminoacetate, polyvinyl alcohol (partially saponified), povidone, fumaric acid, carnauba wax
Prohibition
(Failure to comply may cause worsening of current symptoms or may lead to side effects or accidents)
1. Do not take if you are the following persons
- (1) Persons who have had allergic symptoms caused by this agent or its ingredients
- (2) Persons who have had asthma caused by this agent or other analgesics and antipyretics
- (3) Children under the age of 12
2. Do not take the following medications while taking this medication ︒
- Other cold medications ︑ Analgesics and antipyretics ︑ Sedatives ︑ Cough suppressants ︑ Internal medications containing antihistamines, etc. (internal medications for rhinitis)
3. Do not drive or operate machinery after taking this medication (it may cause drowsiness and other symptoms).
4. Do not take this medication if you are breastfeeding, and avoid breastfeeding while taking this medication.
5. Do not consume alcohol before or after taking ︒
6. Do not take continuously for a long period of time︒
Caution
1. Consult your physician or pharmacist before taking this product if you
- (1) are being treated by a physician or dentist
- (2) are pregnant or at risk of pregnancy
- (3) are elderly
- (4) have had allergies to drugs, etc.
- (5) have a high fever Difficulty urinating
- (6) People diagnosed with thyroid disorder, diabetes, heart disease, hypertension, liver disease, kidney disease, etc. Gastric ulcer︑ Duodenal ulcer︑ Glaucoma︑ Respiratory dysfunction︑ Obstructive sleep apnea syndrome︑ Obesity
Precautions for storage and handling
- Store in a cool, dry place out of direct sunlight.
- Keep this product out of the reach of children.
- Do not replace the container with another one. (This may lead to mishandling or change in quality.)
- Do not handle with wet hands. When water gets on the tablet, the surface may partially dissolve, resulting in discoloration or uneven color. Also, do not pour wet tablets back into the bottle as this may affect other tablets.
- The bottle is filled with product, so please discard it after opening.
- Do not use products that have exceeded their designated expiration date.
