COMPLETE CARE WHOLE MOUTH PROTECTION- sodium fluoride paste, dentifrice 
Church & Dwight Co., Inc.

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.

----------

Arm & Hammer Complete Care Whole Mouth Protection Fluoride Toothpaste

Sodium fluoride 0.24%

(0.15% w/v fluoride ion)

Anticavity toothpaste

aids in the prevention of dental decay

Warnings
Do not use
if irritation occurs and persists.

Do not use if irritation occurs and persists.

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 right away.

Directions

Directions do not swallow • supervise children as necessary until capable of using without supervision • rinse away toothpaste residue throughly after brushing

adults and children 2 years and olderbrush teeth thoroughly after meals or at least twice a day, or use as directed by a dentist or physician
children under 6 yearsinstruct in good brushing and rinsing habits (to minimize swallowing)
children under 2 yearsask a dentist or physician

Water, sodium bicarbonate, sorbitol, hydrated silica, glycerin, tetrasodium pyrophosphate, flavor, sodium lauryl sulfate, sodium lauroyl sarcosinate, poloxamer 407, sodium saccharin, xanthan gum, titanium dioxide

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

Principal Display Panel

Great

New

Formula!

Anticavity

Fluoride

Toothpaste

ARM AND HAMMER The Standard of Purity

UP TO 3X MORE PLAQUE REMOVAL*

COMPLETE CARE™

whole mouth protection

provides deep cleaning, whitening & gum health

fresh mint

ULTRA

SMOOTH

FORMULA

NET WT. 6.0 OZ. (170g)

AH Complete Care Artwork.jpg

COMPLETE CARE WHOLE MOUTH PROTECTION 
sodium fluoride paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10237-675
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
WATER (UNII: 059QF0KO0R)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM PYROPHOSPHATE (UNII: O352864B8Z)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
XANTHAN GUM (UNII: TTV12P4NEE)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
SORBITOL (UNII: 506T60A25R)  
GLYCERIN (UNII: PDC6A3C0OX)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorMINT (Fresh Mint) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10237-675-601 in 1 CARTON12/31/2021
1170 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:10237-675-091 in 1 CARTON12/31/2021
225.5 g in 1 TUBE; Type 0: Not a Combination Product
3NDC:10237-675-121 in 1 CARTON12/31/2021
3340 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35512/31/2021
Labeler - Church & Dwight Co., Inc. (001211952)
Establishment
NameAddressID/FEIBusiness Operations
Church & Dwight Co., Inc.043690812manufacture(10237-675)

Revised: 1/2022
Document Id: d66eac56-a883-8f48-e053-2a95a90aa081
Set id: d00f9d16-de0e-4ffc-e053-2a95a90a2069
Version: 2
Effective Time: 20220125
 
Church & Dwight Co., Inc.