Label: DOCTOR WILL- sodium fluoride, sodium monofluorophosphate paste, dentifrice
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Contains inactivated NDC Code(s)
NDC Code(s): 72531-100-01, 72531-100-02 - Packager: YIRRH HEALTHY LIVING COMPANY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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.
Drug Label Information
Updated October 1, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- active ingredient
- Keep out of reach of children under 6 years of age.
- Purpose
- Uses
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Warnings
When using this product,
if irritation occurs stop use and ask a dentist.
Do not swallow, and rinse enough after use.
Keep out of reach of children under 6 years of age.
If you accidentally swallow more than used for brushing, seek professional assistance or contact a Poison Control Center right away.
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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
- Dr. Will toothpaste
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INGREDIENTS AND APPEARANCE
DOCTOR WILL
sodium fluoride, sodium monofluorophosphate paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72531-100 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 0.05 g in 150 g SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) SODIUM FLUORIDE 0.05 g in 150 g Inactive Ingredients Ingredient Name Strength SORBITOL (UNII: 506T60A25R) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72531-100-02 1 in 1 CARTON 09/17/2018 1 NDC:72531-100-01 150 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 09/17/2018 Labeler - YIRRH HEALTHY LIVING COMPANY (015934472) Registrant - YIRRH HEALTHY LIVING COMPANY (015934472) Establishment Name Address ID/FEI Business Operations Hanil pharmaceutical co.,ltd 688197087 manufacture(72531-100)
