- Active Ingredients
- Purpose
- Keep out of reach of children
- Uses
-
Warnings
For oral use only
Do not use if you have
• glaucoma
• difficulty in urination, prostate disease ( risk of ischuria)
• billiary atresia
• cholelithiasis
• liver disease
• previously experienced sensitivity to this medicationAsk a doctor, dentist, or pharmacist before use if the user takes
• other medication
• reserpine derivatives
• cholagogueStop use and ask a doctor if
• there is no remission of symptoms after several dosages for 2 weeks.Store at cool temperature and dry place with a closed container. Avoid direct sunlight. - Store in a container other than its original container is equivalent to misuse. In order to prevent the reduction of drug efficacy, keep the product in its original container for storage.
This product contains Sodium Benzoate: it may cause minor irritation on skin, eye, and mucous membrane.
- Directions
- Inactive Ingredients
- Galeo
-
INGREDIENTS AND APPEARANCE
GALEO
dihydroxydibutylether liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58354-100 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength 4,4'-OXYDI-2-BUTANOL (UNII: CR6X2Y7NRR) (4,4'-OXYDI-2-BUTANOL - UNII:CR6X2Y7NRR) 4,4'-OXYDI-2-BUTANOL 5 g in 50 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) SORBITOL (UNII: 506T60A25R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58354-100-02 1 in 1 PACKAGE 02/28/2017 1 NDC:58354-100-01 50 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 02/28/2017 Labeler - Cho-A Pharm.Co.,Ltd. (688056831) Registrant - Cho-A Pharm.Co.,Ltd. (688056831) Establishment Name Address ID/FEI Business Operations Cho-A Pharm.Co.,Ltd. 688056831 manufacture(58354-100)