HELLO WHIPPED MELLOW MINT DREAM FLAVOR- sodium monofluorophosphate paste, dentifrice

Hello Whipped Mellow Mint Dream Flavor by

Drug Labeling and Warnings

Hello Whipped Mellow Mint Dream Flavor by is a Otc medication manufactured, distributed, or labeled by Colgate-Palmolive Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Sodium Monofluorophosphate 0.76% (0.14% 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 right away.

Directions

• adults and children 2 years of age and 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

water, calcium carbonate, glycerin, hydrated silica, lauryl glucoside, sodium methyl cocoyl taurate, cellulose gum, benzyl alcohol, sodium carbonate, tetrasodium pyrophosphate, cocamidopropyl betaine, rebaudioside a, acrylates/c10-30 alkyl acrylate crosspolymer, carbomer, sodium bicarbonate, xanthan gum.

Questions?

855-HI-HELLO (1-855-444-3556)

SPL UNCLASSIFIED SECTION

Dist. by Colgate Palmolive Co.,
New York, NY 10022

PRINCIPAL DISPLAY PANEL - 113 g Tube Carton

hello®

whipped
fluoride toothpaste

cavity fighting
+ foaming

mellow mint dream flavor

NET WT 4.0 OZ (113 g)

INGREDIENTS AND APPEARANCE

HELLO WHIPPED MELLOW MINT DREAM FLAVOR 
sodium monofluorophosphate paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 35000-513
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	1.1 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CALCIUM CARBONATE (UNII: H0G9379FGK)
GLYCERIN (UNII: PDC6A3C0OX)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CARBONATE (UNII: 45P3261C7T)
SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
REBAUDIOSIDE A (UNII: B3FUD0528F)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
XANTHAN GUM (UNII: TTV12P4NEE)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor	MINT	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 35000-513-10	1 in 1 CARTON	01/01/2026
1		113 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 DRUG	M021	01/01/2026

Labeler - Colgate-Palmolive Company (001344381)