AIM CAVITY PROTECTION MULTI BENEFIT- sodium fluoride paste, dentifrice

AIM Cavity Protection by

Drug Labeling and Warnings

AIM Cavity Protection by is a Otc medication manufactured, distributed, or labeled by Church & Dwight Co., Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients
Sodium fluoride (0.24%)

PURPOSE

Purpose
Anticavity toothpaste

INDICATIONS & USAGE

Use  aids in the prevention of dental decay

KEEP OUT OF REACH OF CHILDREN

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

WARNINGS

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

DOSAGE & ADMINISTRATION

Directions

• do not swallow
• supervise children as necessary until capable of using without supervision
• 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 :instruct in good brushing and rinsing habits (to minimize swallowing)
• children under 2 years: ask a dentist or physician

INACTIVE INGREDIENT

Inactive ingredients  sorbitol, water, hydrated silica, PEG-8, sodium lauryl sulfate, SD alcohol 38-B, flavor, cellulose gum, sodium saccharin, titanium dioxide.

QUESTIONS

Questions or comments?  Call 1-800-786-5135 Monday-Friday 9am-5pm ET

Principal Display Panel

Take AIM Against Cavities

AIM

Cavity Protection

Ultra Mint PASTE

NET WT. 6 OZ. (170g) Anticavity Fluoride MULTI BENEFIT Cleans Freshens

Toothpaste Protects

INGREDIENTS AND APPEARANCE

AIM CAVITY PROTECTION  MULTI BENEFIT
sodium fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10237-638
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	2.4 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
SORBITOL (UNII: 506T60A25R)
WATER (UNII: 059QF0KO0R)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
ALCOHOL (UNII: 3K9958V90M)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10237-638-60	1 in 1 CARTON	08/01/2015	09/26/2019
1		170 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 10237-638-55	1 in 1 CARTON	08/01/2015
2		156 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	part355	08/04/2011

Labeler - Church & Dwight Co., Inc. (001211952)

Establishment
Name	Address	ID/FEI	Business Operations
Church & Dwight Co., Inc.		043690812	manufacture(10237-638)