BABYSONS

Product NDC: 73519-001
11-digit product format: 735190001
Labeler code: 73519
Product ID: 73519-001_25cb134c-b31f-af58-e063-6394a90adbb7
Type: HUMAN OTC DRUG
Nonproprietary name: DEXPANTHENOL
Dosage form: OINTMENT
Route: TOPICAL
Labeler: Laboratorios Quimica Son's, S.A. de C.V
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2020-06-15
Substance: DEXPANTHENOL
Active strength: 50 mg/g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: BABYSONS
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
DEXPANTHENOL	50 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1O6C93RI7Z	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
249792	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
8a4782fc-5917-4f63-b9bf-6597be2afc6c	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73519-001-30	2023-02-03	C162847	48780-1	f386c649-efb2-0266-e053-dadaa90a7c1a	BABYSONS
73519-001-30	2023-01-30	C162847	48780-1	f386c649-efb2-0266-e053-dadaa90a7c1a	BABYSONS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73519-001-30	BABYSONS	30 g in 1 TUBE	OINTMENT	30		4
73519-001-30	BABYSONS	1 in 1 BOX	OINTMENT	1		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73519-001	BABYSONS (DEXPANTHENOL) OINTMENT [LABORATORIOS QUIMICA SON'S, S.A. DE C.V]	4	Current NDC, Legacy NDC, 2 package rows	20241102_8a4782fc-5917-4f63-b9bf-6597be2afc6c.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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
BABYSONS	DEXPANTHENOL	Laboratorios Quimica Son's, S.A. de C.V	8a4782fc-5917-4f63-b9bf-6597be2afc6c	2024-10-31	Warnings	Exact identifier ndc (product): 73519-001

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
1O6C93RI7Z	DEXPANTHENOL	81-13-0	DEXPANTHENOL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
249792	dexpanthenol 5 % Topical Ointment	PSN	8a4782fc-5917-4f63-b9bf-6597be2afc6c	4
249792	dexpanthenol 0.05 MG/MG Topical Ointment	SCD	8a4782fc-5917-4f63-b9bf-6597be2afc6c	4
249792	dexpanthenol 5 % Topical Ointment	SY	8a4782fc-5917-4f63-b9bf-6597be2afc6c	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
73519-001-30	73519000130	1 TUBE in 1 BOX (73519-001-30) / 30 g in 1 TUBE	1 tube	2020-06-15	0000-00-00	No	No	Current