COMPLETE CARE PLUS ENAMEL STRENGTHENING- sodium fluoride paste, dentifrice

Complete Care by

Drug Labeling and Warnings

Complete Care 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

Warning

Do not use if irritation occur s and persists.
_________________________________________________

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
                           rinse away toothpaste residue thoroughly after brushing

adults and children 2 years and older           brush teeth throughly 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                                    consult a dentist or physician

INACTIVE INGREDIENT

Inactive ingredients   sodium bicarbonate, PEG/PPG-38/8 copolymer, PEG/PPG-116/66 copolymer, calcium sulfate, silica, sodium lauryl sulfate, flavor, PEG-8, dipotassium phosphate, sodium saccharin,sodium carbonate peroxide.

QUESTIONS

Questions or comments?  Call 1-800-786-5135 Monday-Friday 9am-5pm ET or visit www.myoralcare.com

Principal Display Panel

ARM AND HAMMER The Standard of Purity

Fluoride Anti-Cavity Toothpaste FRESH MINT FLAVOR

COMPLETE CARE

Plus Enamel Strengthening Liquid Calcium and Fluoride

NET WT. 6.0 OZ. (170g)

INGREDIENTS AND APPEARANCE

COMPLETE CARE  PLUS ENAMEL STRENGTHENING
sodium fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10237-654
Route of Administration	DENTAL

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

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
POLOXALENE (UNII: V8B3K56SW0)
CALCIUM SULFATE (UNII: WAT0DDB505)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
PHOSPHATE ION (UNII: NK08V8K8HR)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SODIUM CARBONATE (UNII: 45P3261C7T)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)

Product Characteristics
Color	white	Score
Shape		Size
Flavor	MINT (Fresh Mint)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10237-654-60	1 in 1 CARTON	01/29/2012	11/11/2022
1		170 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	01/29/2012	11/11/2022

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

Establishment
Name	Address	ID/FEI	Business Operations
Church & Dwight Co., Inc.		043690812	manufacture(10237-654)