BOP WHITENINGTOOTHPASTE- bop whitening toothpaste gel

Country: United States

Language: English

Source: NLM (National Library of Medicine)

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Active ingredient:

GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) (GLYCYRRHIZIN - UNII:6FO62043WK), XYLITOL (UNII: VCQ006KQ1E) (XYLITOL - UNII:VCQ006KQ1E)

Available from:

Shanghai Gemang Trading Co., Ltd.

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

Anticavity Anti-inflammatory Help protect against cavities and diminish inflammation.

Authorization status:

unapproved drug other

Summary of Product characteristics

                                BOP WHITENINGTOOTHPASTE- BOP WHITENING TOOTHPASTE GEL
SHANGHAI GEMANG TRADING CO., LTD.
_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._
----------
XYLITOL
GLYCYRRHIZINATE DIPOTASSIUM
Sorbitol Hydrated silica, Water, Sodium Lauroyl Sarcosinate,Sodium
Phytate,
Polyethylene Glycol 1600,Hydroxyapatite,Menthol,
sucralose,Hyaluronate Sodium,Chondrus Crispus Carrageenan,Pistacia
Lentiscus
Resin,Menthone 1,2-Glycerol
Ketal,Hydroxyacetophenone, Caprylyl Glycol,1,2-Hexanediol,Sodium
Phpsphate,Titanium
Dioxide.
Keep out of reach of children under 6 yrs. of age.
Anticavity
Anti-inflammatory
USE
Help protect against cavities and diminish inflammation.
DIRECTIONS
Adults and children 2 yrs.& older: brush teeth thoroughly aftermeals
or at least twice a
day or use as directed by a dentist.
Do not swallow.
To minimize swallowing use a pea-sized amount in children under 6.
Supervise children's brushing until good habits are established.
Children under 2 yrs.: ask a dentist.
Store in a dry and cool place.
Keep out of reach of children under 6 yrs. of age. If more than used
for brushing is
accidentally swallowed, get medical help or contact a Poison Control
Center right away
BOP WHITENINGTOOTHPASTE
bop whitening toothpaste gel
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:82574-001
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) (GLYCYRRHIZIN -
UNII:6FO62043WK)
GLYCYRRHIZ INATE
DIPOTASSIUM
0.3 g
in 100 g
XYLITOL (UNII: VCQ006KQ1E) (XYLITOL - UNII:VCQ006KQ1E)
XYLITOL
3 g
in 100 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
SODIUM PHOSPHATE (UNII: SE337SVY37)
PHYTATE SODIUM (UNII: 88496G1ERL)
POLYETHYLENE GLYCOL 1600 (UNII: 1212Z7S33A)
TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
5-METHYL-1,3,5-TRIPHENYL-2-PYRAZOLINE (UNII: 96K6O83026)
HYALURONATE SODIUM (UNII: YSE9P
                                
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