DAWNMIST FLUORIDE sodium monofluorophosphate paste

Land: USA

Språk: engelska

Källa: NLM (National Library of Medicine)

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Produktens egenskaper Produktens egenskaper (SPC)
15-01-2018

Aktiva substanser:

SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (MONOFLUOROPHOSPHATE ION - UNII:4964UZ79MI)

Tillgänglig från:

Dukal Corporation

INN (International namn):

SODIUM MONOFLUOROPHOSPHATE

Sammansättning:

SODIUM MONOFLUOROPHOSPHATE 0.76 g in 100 g

Receptbelagda typ:

OTC DRUG

Bemyndigande status:

OTC monograph final

Produktens egenskaper

                                DAWNMIST FLUORIDE - SODIUM MONOFLUOROPHOSPHATE PASTE
DUKAL CORPORATION
_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._
----------
DAWNMIST(R) ANTICAVITY FLUORIDE TOOTHPASTE
ACTIVE INGREDIENT
Sodium Monofluorophosphate 0.76 percent
PURPOS E
Anticavity
US E
Aids in the prevention of dental cavities.
KEEP OUT OF REACH OF CHILDREN
under 6 years of age
WARNING
If you accidentally swallow more than used for brushing seek
professional assistance or contact a
Poison Control Center immediately.
DIRECTIONS
Adults and children 2 years and older: Brush teeth thoroughly after
meals or at least twice a day or use
as directed by a dentist or physician.
Children under 6 years: To minimize swallowing use a pea sized amount
and supervise brushing until
good habits are established.
Children under 2 years: Ask a dentist or physician.
INACTIVE INGREDIENTS
Calcium Carbonate, Water, Sorbitol, Hydrated Silica, Glycerin, Sodium
Lauryl Sulfate, Flavor,
Tetrasodium Pyrophosphate, Cellulose Gum, Sodium Benzoate, Sodium
Saccharin
PACKAGE LABEL
DawnMist (R)
Anticavity Fluoride Toothpaste
Cavity Fighting Formula
Fresh Minty Taste
Expiration Date: Expiration Date on Crimp of Tube.
Manufactured for:
DUKAL CORPORATION
Ronkonkoma, NY 11779
(631) 656-3800
Made in Malaysia
DAWNMIST FLUORIDE
sodium monofluorophosphate paste
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:6 5517-10 0 0
ROUTE OF ADMINISTRATION
DENTAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
SO DIUM MO NO FLUO RO PHO SPHATE (UNII: C8 10 JCZ56 Q)
(MONOFLUOROPHOSPHATE ION - UNII:49 6 4UZ79 MI)
SODIUM
MONOFLUOROPHOSPHATE
0 .76 g
in 10 0 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
CALCIUM CARBO NATE (UNII: H0 G9 379 FGK)
WATER (UNII: 0 59 QF0 KO0 R)
SO RBITO L (UNII: 50 6 T6 0 A25R)
HYDRATED SILICA (UNII: Y6 O7T4G8 P9 )
GLYCERIN (UNII: PDC6 A3C0 OX)
SO DIUM LAURYL SU
                                
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