Aquafresh description, usages, side effects, indications, overdosage, supplying and lots more!

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Aquafresh

GlaxoSmithKline Consumer Healthcare LP

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Sodium monofluorophosphate (0.15% w/v fluoride ion)

Anticavity

aids in the prevention of dental cavities

When using this product,

if irritation occurs discontinue use.

Keep out of the reach of children under 6 years of age.

If you accidentally swallow more than used for brushing, get medical help or contact a Poison Control Center right away.

  • adults and children 2 years and older
    • ∘apply toothpaste onto a toothbrush
    • ∘brush teeth thoroughly, preferably after each meal, at least twice a day, and not more than 3 times a day, or as directed by a dentist or doctor. Minimize swallowing. Spit out after brushing.
    • ∘to minimize swallowing for children under 6 years of age, use a pea-sized amount and supervise brushing and rinsing until good habits are established
  • children under 2 years of age: consult a dentist or doctor.
  • •store below 25°C (77°F)

sorbitol, calcium carbonate, water, hydrated silica, glycerin, PEG-8, flavor, sodium lauryl sulfate, cellulose gum, titanium dioxide, sodium bicarbonate, sodium saccharin, calcium carrageenan, sodium benzoate, D&C red #30

sorbitol, water, calcium carbonate, hydrated silica, glycerin, PEG-8, flavor, sodium lauryl sulfate, cellulose gum, titanium dioxide, sodium bicarbonate, sodium saccharin, sodium benzoate, calcium carrageenan, blue 1 lake, red 30 lake

sorbitol, water, calcium carbonate, hydrated silica, glycerin, PEG-8, flavor, sodium lauryl sulfate, cellulose gum, titanium dioxide, sodium bicarbonate, sodium saccharin, calcium carrageenan, sodium benzoate, blue 1 lake, red 30 lake

call toll-free 1-800-897-5623 (English/Spanish) weekdays

Principal Display Panel

NDC 0135-0442-01

Aquafresh kids

FLUORIDE TOOTHPASTE

TRIPLE PROTECTION

bubble fresh

NET WT. 4.6 oz (130.4g)

ADA Accepted American Dental Association®

Aquafresh fights cavities with fluoride...

freshens breath...

and has a great bubble fresh taste, in one complete toothpaste.

www.Aquafresh.com

Aqua®, Aquafresh®, Triple Protection®, and various design elements are trademarks of the GlaxoSmithKline group of companies.

This product contains no sugar.

"The ADA Council on Scientific Affairs' Acceptance of Aquafresh Kids is based on its finding that the product is effective in helping to prevent and reduce tooth decay, when used as directed."

©2009 GlaxoSmithKline

GlaxoSmithKline Consumer Healthcare, L.P.

Moon Township, PA 15108

Made in England

From the Aqua® family of products.

30050XC

Principal Display Panel

NDC 0135-0126-02

Aquafresh®

kids

Fluoride Toothpaste

Cavity Protection

BUBBLE MINT

2+ years

ADA Accepted American Dental Association®

NET WT. 4.6 oz (130.4g)

Aquafresh toothpaste fights cavities with fluoride...

freshens breath...

and has a great bubble mint taste, in one complete toothpaste.

ALWAYS FOLLOW THE LABEL

This product contains no sugar, like all ADA-accepted toothpastes.

Aquafresh, the iconic nurdle device and other marks are trademarks of the GlaxoSmithKline group of companies.

Note: If pump doesn't work, hold button down and firmly push up inside base.

"The ADA Council on Scientific Affairs' Acceptance of Aquafresh Kids is based on its finding that the product is effective in helping to prevent and reduce tooth decay, when used as directed."

GlaxoSmithKline

Consumer Healthcare, L.P.

Moon Township, PA 15108

www.aquafresh.com

©2013 GlaxoSmithKline

100023XC

Principal Display Panel

NDC 0135-0534-08

Aquafresh®

kids

Fluoride Toothpaste

CAVITY PROTECTION

2+ YEARS

fresh ‘n fruity

NET WT. 4.6 oz (130.4g)

Aquafresh® toothpaste fights cavities with fluoride…

freshens breath…

and has a great fresh and fruity flavor, in one complete toothpaste

ALWAYS FOLLOW THE LABEL

www.Aquafresh.com

AQUAFRESH, TRIPLE PROTECTION, the iconic Nurdle device and other marks are trademarks of the GlaxoSmithKline group of companies.

Distributed by

GlaxoSmithKline

Consumer Healthcare, L.P.

Moon Township, PA 15108

Made in England

©2013 GlaxoSmithKline

100999XC

Aquafresh

sodium monofluorophosphate PASTE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0135-0442
Route of Administration DENTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM MONOFLUOROPHOSPHATE FLUORIDE ION 1.10 mg

Inactive Ingredients

Ingredient Name Strength
sorbitol
CALCIUM CARBONATE
water
HYDRATED SILICA
GLYCERIN
polyethylene glycol 400
SODIUM LAURYL SULFATE
CARBOXYMETHYLCELLULOSE SODIUM
titanium dioxide
SODIUM BICARBONATE
saccharin sodium
CARRAGEENAN
SODIUM BENZOATE
D&C RED NO. 30

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 130.4 in 1 TUBE
2 NDC:0135-0442-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 2011-01-28


Aquafresh

sodium monofluorophosphate PASTE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0135-0126
Route of Administration DENTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM MONOFLUOROPHOSPHATE FLUORIDE ION 1.10 mg

Inactive Ingredients

Ingredient Name Strength
sorbitol
water
CALCIUM CARBONATE
HYDRATED SILICA
GLYCERIN
polyethylene glycol 400
SODIUM LAURYL SULFATE
CARBOXYMETHYLCELLULOSE SODIUM
titanium dioxide
SODIUM BICARBONATE
saccharin sodium
CARRAGEENAN
SODIUM BENZOATE
FD&C BLUE NO. 1
D&C RED NO. 30

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0135-0126-02 130.4 in 1 CAN
2 119 in 1 TUBE
3 22.7 in 1 TUBE
4 NDC:0135-0126-08 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 2011-01-28


Aquafresh

sodium monofluorophosphate PASTE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0135-0534
Route of Administration DENTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM MONOFLUOROPHOSPHATE FLUORIDE ION 1.10 mg

Inactive Ingredients

Ingredient Name Strength
sorbitol
water
CALCIUM CARBONATE
HYDRATED SILICA
GLYCERIN
polyethylene glycol 400
SODIUM LAURYL SULFATE
CARBOXYMETHYLCELLULOSE SODIUM
titanium dioxide
SODIUM BICARBONATE
saccharin sodium
CARRAGEENAN
SODIUM BENZOATE
FD&C BLUE NO. 1
ALUMINUM OXIDE
D&C RED NO. 30

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 130.4 in 1 TUBE
2 22.7 in 1 TUBE
3 NDC:0135-0534-07 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 2012-03-09


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