Label: BAMBOO SALT 160G- sodium lauryl sulfate paste, dentifrice
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Contains inactivated NDC Code(s)
NDC Code(s): 69642-1400-1, 69642-1400-2 - Packager: Hanul Trading Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated June 24, 2017
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredient: Sorbitol Solution, Water(Aqua), Hydrated Silica, Flavor(Aroma), PEG-6, Xanthan Gum, Cellulose Gum, Poloxamer 407, Sodium Saccharin, Methyl Paraben, Sodium Chloride, Tocopheryl Acetate, Sodium Bisulfite, Camelia Sinensis Leaf Extract, D&C Yellow NO.10(CI47005), FD&C Blue No.1 (CI 42090)
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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Direction
Direction: Adults and children 6 years of age and older: Brush teeth thoroughly preferably after each meal or at least twice a day, or as directed by a dentist or doctor, Instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing). Supervise children as necessary until capable of using without supervision. Children under 6 years of age: Consult a dentist or doctor
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Direction
Direction: Adults and children 6 years of age and older: Brush teeth thoroughly preferably after each meal or at least twice a day, or as directed by a dentist or doctor, Instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing). Supervise children as necessary until capable of using without supervision. Children under 6 years of age: Consult a dentist or doctor
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BAMBOO SALT 160G
sodium lauryl sulfate paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69642-1400 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM LAURYL SULFATE (UNII: 368GB5141J) (LAURYL SULFATE - UNII:DIQ16UC154) SODIUM LAURYL SULFATE 1.21 g in 160 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69642-1400-2 1 in 1 CARTON 06/10/2015 06/24/2017 1 NDC:69642-1400-1 160 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 03/19/2015 Labeler - Hanul Trading Co., Ltd. (689512982) Registrant - Hanul Trading Co., Ltd. (689512982) Establishment Name Address ID/FEI Business Operations KOCO TRADING CO., INC. 079457993 repack(69642-1400) Establishment Name Address ID/FEI Business Operations LG Household&Health Care 688276187 manufacture(69642-1400) Establishment Name Address ID/FEI Business Operations Hanul Trading Co., Ltd. 689512982 relabel(69642-1400)
