Maxixum Security Gel Toothpaste description, usages, side effects, indications, overdosage, supplying and lots more!

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Maxixum Security Gel Toothpaste

Dabur India Limited

MAXIMUM SECURITY® GEL TOOTHPASTE


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

NET WT 0.15 OZ

DRUG FACTS:

ACTIVE INGREDIENT

Sodium fluoride- 0.22% (0.1% w/v fluoride ion)

PURPOSE

Anticavity.

USE

Helps protect against cavities.

WARNINGS

Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center immediately.

DIRECTIONS:

Adults & Children 6 years of age & older:

Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician.

Children 2 to 6 years:

Use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing).

Children under 2 years:

Ask a dentist or physician.

INACTIVE INGREDIENTS

Purified Water, Sorbitol, Carbopol, Sodium Lauryl Sulphate, Flavor, Poly Ethylene Glycol 1500, Sodium Saccharin, Precipitated Silica, Sodium Carboxy Methyl Cellulose, Methyl Paraben, Propyl Paraben.

Product of India,
Exclusive Distributor:
Bob Barker Co. Inc.,
Phone: 1-800-334-9880.
Expires: 3 years from the Date of Mfg.

C.No. DNH/COS/DNH/52
Mfg. Date & Batch No. on crimp.

24.06.2009

MAXIMUM SECURITY GEL TOOTHPASTE
ACTIVE INGREDIENT: SODIUM FLUORIDE - 0.22 %
(0.1% w/v fluoride Ion)
SR. NO. INGREDIENTS

  • Treated water
  • Sorbitol
  • Carbopol
  • Sodium lauryl sulphate
  • Flavor
  • Polyethylene glycol 1500
  • Sodium saccharin
  • Precipitated Silica
  • Sodium Carboxy Methyl Cellulose
  • Methyl Paraben
  • Propyl Paraben

Principal Display Panel

Packet Label
TEAR HERE
MAXIMUM SECURITY®
GEL TOOTHPASTE
NET WT 0.15 OZ

Maxixum Security Gel Toothpaste

Fluoride Toothpaste PASTE, DENTIFRICE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68747-6028
Route of Administration DENTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION 2.2 mg

Inactive Ingredients

Ingredient Name Strength
water
sorbitol
CARBOMER HOMOPOLYMER TYPE C
SODIUM LAURYL SULFATE
POLYETHYLENE GLYCOL 1500
saccharin sodium
SILICON DIOXIDE
CARBOXYMETHYLCELLULOSE SODIUM
METHYLPARABEN
PROPYLPARABEN

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68747-6028-1 4.2 in 1 PACKET

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 2009-08-25


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Be sure to consult your doctor before taking any medication!
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