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NDC 51206-0312-02 Opal by Opalescence Original 1.1 mg/g Details

Opal by Opalescence Original 1.1 mg/g

Opal by Opalescence Original is a DENTAL GEL, DENTIFRICE in the HUMAN OTC DRUG category. It is labeled and distributed by Ultradent Products, Inc.. The primary component is SODIUM FLUORIDE.

MedlinePlus Drug Summary

Fluoride is used to prevent tooth decay. It is taken up by teeth and helps to strengthen teeth, resist acid, and block the cavity-forming action of bacteria. Fluoride usually is prescribed for children and adults whose homes have water that is not fluoridated (already has fluoride added). This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 51206-0312-02
Last Updated: 04/14/2024
MedLinePlus Full Drug Details: Fluoride

Product Information

NDC	51206-0312
Product ID	51206-312_1a82543f-9648-467e-948e-b0a8350209f2
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Opal by Opalescence Original
Proprietary Name Suffix	n/a
Non-Proprietary Name	Sodium Fluoride
Product Type	HUMAN OTC DRUG
Dosage Form	GEL, DENTIFRICE
Route	DENTAL
Active Ingredient Strength	1.1
Active Ingredient Units	mg/g
Substance Name	SODIUM FLUORIDE
Labeler Name	Ultradent Products, Inc.
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH DRUG
Application Number	M021
Listing Certified Through	2024-12-31

Package

NDC 51206-0312-02 (51206031202)

Pricing Information	N/A
NDC Package Code	51206-312-02
Billing NDC	51206031202
Package	3 CARTON in 1 PACKAGE, COMBINATION (51206-312-02) / 1 TUBE in 1 CARTON (51206-312-01) / 133 g in 1 TUBE
Marketing Start Date	2023-11-19
NDC Exclude Flag	N