Label: JANGDAEWON PROBIOTICS- lactobacillus rhamnosus powder
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Contains inactivated NDC Code(s)
NDC Code(s): 72460-600-01, 72460-600-02 - Packager: Daewon Pharmaceutical Co., Ltd.
- 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.
Drug Label Information
Updated March 13, 2019
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
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WARNINGS
Warnings
■ Pregnant of lactating women or who takes other medicines need to consult a professional before taking this product.
■ Idiosyncratic or allergic person need to decide to take this product after consulting a doctor
■ In case of abnormal symptom, stop taking this product and consult a medical doctor or inquire to customer service.
■ Make sure to check expiry date, and please follow suggested use instruction.
■ Avoid direct ray of light and keep in cool and dry place, and keep out of the child's reach.
■ Consume this product as soon as opening, owing to the possibility of moisture absorption. - KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
JANGDAEWON PROBIOTICS
lactobacillus rhamnosus powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72460-600 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Lactobacillus rhamnosus (UNII: 9601IVB87J) (LACTOBACILLUS RHAMNOSUS - UNII:9601IVB87J) Lactobacillus rhamnosus 30 mg in 2 g Inactive Ingredients Ingredient Name Strength Bifidobacterium longum (UNII: 831AQW699W) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72460-600-02 30 in 1 BOX 02/01/2019 1 NDC:72460-600-01 2 g in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 02/01/2019 Labeler - Daewon Pharmaceutical Co., Ltd. (689275501) Registrant - Daewon Pharmaceutical Co., Ltd. (689275501) Establishment Name Address ID/FEI Business Operations Daewon Pharmaceutical Co., Ltd. 689275501 manufacture(72460-600)