Label: LINGTEA- taurine powder
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Updated June 24, 2018
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
Use under medical supervision.
For children under 12 months, consult your doctor regarding appropriate use.
Notify your doctor immediately if vomiting, diarrhea, decreased urination or other signs of dehydration continue beyond 24 hours.
Talk to your doctor before using Lingtea if you have heart or kidney disease, electrolyte or fluid restrictions
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72355-0001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TAURINE (UNII: 1EQV5MLY3D) (TAURINE - UNII:1EQV5MLY3D) TAURINE 1 g in 100 g Inactive Ingredients Ingredient Name Strength SUCRALOSE (UNII: 96K6UQ3ZD4) SODIUM CITRATE (UNII: 1Q73Q2JULR) ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72355-0001-1 11.255 g in 1 POUCH; Type 0: Not a Combination Product 06/25/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/25/2018 Labeler - LINGER WATER (694892011) Registrant - LINGER WATER (694892011) Establishment Name Address ID/FEI Business Operations ESoo Bio Co., Ltd 694086456 manufacture(72355-0001) Establishment Name Address ID/FEI Business Operations LINGER WATER 694892011 pack(72355-0001) , label(72355-0001)