Label: DR DEEP DEEP FRESH- glycerin paste, dentifrice
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Contains inactivated NDC Code(s)
NDC Code(s): 76015-110-01 - Packager: MineralHouse Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 August 12, 2016
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- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PURPOSE
- WARNINGS
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- STORAGE AND HANDLING
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INACTIVE INGREDIENT
Inactive Ingredients: Aluminum Chlorohydroxy Allantoinate, Aminocaproic Acid, D-Sorbitol Solution, Polyethylene Glycol 4000, stevgiol Glycoside, Xylitol, Citrus Paradisi (Grapefruit) Seed Extract, Camellia Sinensis Leaf Extract, Sodium Carboxymethyl Cellulose, Cacamidopropyl Betaine, L-Menthol, Mentha Piperita (Peppermint) Oil, Aqua
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INGREDIENTS AND APPEARANCE
DR DEEP DEEP FRESH
glycerin paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76015-110 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 7.68 g in 120 g Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) 4.8 g in 120 g ALCLOXA (UNII: 18B8O9DQA2) AMINOCAPROIC ACID (UNII: U6F3787206) SORBITOL (UNII: 506T60A25R) POLYETHYLENE GLYCOL 4000 (UNII: 4R4HFI6D95) XYLITOL (UNII: VCQ006KQ1E) CITRUS PARADISI SEED (UNII: 12F08874Y7) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) LEVOMENTHOL (UNII: BZ1R15MTK7) MENTHA PIPERITA (UNII: 79M2M2UDA9) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76015-110-01 1 in 1 PACKAGE 08/12/2016 1 120 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 final part347 08/12/2016 Labeler - MineralHouse Corporation (557802539) Registrant - MineralHouse Corporation (557802539) Establishment Name Address ID/FEI Business Operations MineralHouse Corporation 557802539 relabel(76015-110) , repack(76015-110) Establishment Name Address ID/FEI Business Operations Sangleaf Pharm., Co. Ltd. 689847343 manufacture(76015-110)