Orajel Kids Superman

Product NDC: 10237-732
11-digit product format: 102370732
Labeler code: 10237
Product ID: 10237-732_574b93ff-4959-9da6-e063-6394a90acff7
Type: HUMAN OTC DRUG
Nonproprietary name: Anticavity Toothpaste
Dosage form: GEL, DENTIFRICE
Route: DENTAL
Labeler: Church & Dwight Co., Inc.
Application: M021
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2025-01-07
Substance: SODIUM FLUORIDE
Active strength: 1.5 mg/g
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: Orajel Kids Superman
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SODIUM FLUORIDE	1.5 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
8ZYQ1474W7	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
416783	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
2b47af33-32d4-7c06-e063-6394a90a2f33	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6084a4f4-5437-c9a5-caec-5361ee075a59	Product name	1	20140508
90c5639a-61b0-88d6-ddcf-21888e94869a	Product name	1	20140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10237-732-42	Orajel Kids Superman	119 g in 1 TUBE	GEL, DENTIFRICE	119		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10237-732	ORAJEL KIDS SUPERMAN (ANTICAVITY TOOTHPASTE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.]	1	Current NDC, 1 package rows	20250112_2b47af33-32d4-7c06-e063-6394a90a2f33.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 32 of 51 · 1,013 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Listerine Total Care Kids Anticavity Fluoride Rinse - Berry Splash	SODIUM FLUORIDE	Kenvue Brands LLC	28986d7f-3e9a-8dfb-e063-6394a90a731e	2025-12-10	Warnings	Exact identifier application number: M021
Toms of Maine Tropical Island	ALUMINUM CHLOROHYDRATE	Colgate-Palmolive Company	0d6c51bc-5391-4533-b4fd-961dc4f36342	2025-12-10	Warnings	Exact identifier application number: M021
Business Class Kit	SODIUM MONOFLUOROPHOSPHATE	American Airlines, Inc.	483d7aec-34ac-49c5-ac0e-8fba5b4737ae	2025-12-09	Warnings	Exact identifier application number: M021
Colgate Anticavity Kit	SODIUM MONOFLUOROPHOSPHATE	Ming Fai Industrial (Shenzhen) Co. Ltd	121decce-c364-4060-87da-0c6a6cd48474	2025-12-08	Warnings	Exact identifier application number: M021
First Class Kit	SODIUM MONOFLUOROPHOSPHATE	American Airlines, Inc.	ba717de8-c3a2-41bf-85a1-aa75f9744d30	2025-12-08	Warnings	Exact identifier application number: M021
United Airlines Business Class Kit	SODIUM MONOFLUOROPHOSPHATE	United Airlines	94c5e9a4-19f3-4590-9da4-313c75261231	2025-12-08	Warnings	Exact identifier application number: M021
Dr. Jen SuperPaste Nano-Hydroxyapatite	SODIUM FLUORIDE	Dr Jen Natural, LLC	5f08d994-e458-42b2-aa39-e84fca3acf48	2025-12-05	Warnings	Exact identifier application number: M021
Colgate Anticavity Kit	SODIUM MONOFLUOROPHOSPHATE	Ming Fai Industrial (Shenzhen) Co. Ltd	86dfd09d-f3b6-4c4b-852d-7e04dc5c8fec	2025-12-05	Warnings	Exact identifier application number: M021
Dr. Jen SuperPaste Nano-Hydroxyapatite	SODIUM FLUORIDE	Dr Jen Natural, LLC	8b28b857-9162-4065-b0a0-571efffe9787	2025-12-05	Warnings	Exact identifier application number: M021
Dr. Jen SuperPaste Ortho	SODIUM FLUORIDE	Dr Jen Natural, LLC	9dd248bf-9488-43cd-a041-e8315a05ce5d	2025-12-04	Warnings	Exact identifier application number: M021
Dr. Jen SuperPaste Perio	SODIUM FLUORIDE	Dr Jen Natural, LLC	8c7e6d3a-49d9-4098-9d5e-e9792b373574	2025-12-04	Warnings	Exact identifier application number: M021
Colgate Total Plaque Cleanse	STANNOUS FLUORIDE	Colgate-Palmolive Company	b2980238-5bcb-467f-9e90-a307938632c2	2025-12-03	Warnings	Exact identifier application number: M021
Advance White Extreme Whitening Tartar Control	SODIUM FLUORIDE	Church & Dwight Co., Inc.	b539264f-e1ff-440b-af76-84266fe2c0a2	2025-12-02	Warnings	Exact identifier application number: M021
Sensodyne Pronamel Clinical Enamel Strength Fresh Breath	POTASSIUM NITRATE, SODIUM FLUORIDE	Haleon US Holdings LLC	34a1a32e-3017-f018-e063-6394a90a0230	2025-12-01	Warnings	Exact identifier application number: M021
Freshmint Anticavity Fluoride	SODIUM MONOFLUOROPHOSPHATE	New World Imports, Inc	77e51d6f-c1a2-4650-b3dd-5e4552379e77	2025-12-01	Warnings	Exact identifier application number: M021
Freshmint Sensitive	POTASSIUM NITRATE AND SODIUM FLUORIDE	New World Imports, Inc	aa2e0864-3325-4acf-a2c5-0eb27eb18baf	2025-12-01	Warnings	Exact identifier application number: m021
PRO-SYS	SODIUM FLUORIDE AND POTASSIUM NITRATE	Benco Dental	4e470ba4-60bb-1815-e063-6294a90abacc	2025-12-01	Warnings	Exact identifier application number: M021
PRO-SYS	SODIUM FLUORIDE	Benco Dental	4e539cb2-bcbd-95fc-e063-6294a90a2121	2025-12-01	Warnings	Exact identifier application number: M021
Cool sense Care Plus	SODIUM FLUORIDE	DONG IL PHARMS CO., LTD.	44763bf6-caf3-ec69-e063-6394a90a0ee1	2025-11-25	Warnings	Exact identifier application number: M021
DOCTRUST DOUBLEX Tooth	SODIUM FLUORIDE	DONG IL PHARMS CO.,LTD	44765e86-2eb2-6381-e063-6394a90a761f	2025-11-25	Warnings	Exact identifier application number: M021

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
8ZYQ1474W7	SODIUM FLUORIDE	7681-49-4	SODIUM FLUORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
416783	sodium fluoride 0.24 % Toothpaste	PSN	2b47af33-32d4-7c06-e063-6394a90a2f33	1
416783	sodium fluoride 0.0024 MG/MG Toothpaste	SCD	2b47af33-32d4-7c06-e063-6394a90a2f33	1
416783	sodium fluoride 0.24 % (fluoride ion 0.13 % ) Toothpaste	SY	2b47af33-32d4-7c06-e063-6394a90a2f33	1
416783	sodium fluoride 0.24 % (fluoride ion 0.14 % ) Toothpaste	SY	2b47af33-32d4-7c06-e063-6394a90a2f33	1
416783	sodium fluoride 0.24 % (fluoride ion 0.15 % ) Toothpaste	SY	2b47af33-32d4-7c06-e063-6394a90a2f33	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
10237-732-42	10237073242	119 g in 1 TUBE (10237-732-42)	119 g	2025-01-07	No	No	Current
10237-732-44	10237073244	4 TUBE in 1 BOX (10237-732-44) / 119 g in 1 TUBE	4 tube	2025-08-01	No	No	Current