Odorono

Product NDC: 51048-202
Requested package NDC: 51048-202-25
11-digit product format: 510480202
Labeler code: 51048
Product ID: 51048-202_2c80c6dc-485c-4847-b5b8-a39d9ab74563
Type: HUMAN OTC DRUG
Nonproprietary name: Aluminum Chlorohydrate
Dosage form: LIQUID
Route: TOPICAL
Labeler: Omega & Delta Co
Application: part350
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2006-05-08
Marketing end: 0000-00-00
Substance: ALUMINUM CHLOROHYDRATE
Active strength: 20 g/100mL
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	51048-202	51048-202-25	I	Inactivated by FDA		2026-10-15

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 1 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	51048-202	51048-202-25	I	Inactivated by FDA		excluded / ndc_excluded.zip	`9bebd1f3094a…`	`5416666fcb17…`

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51048-202-25	2020-11-12	C162847	48780-1	9d75b9d0-5122-f424-e053-dadaa90a57ce	Odorono Antiperspirant Deodorant Roll-on Powder
51048-202-25	2020-01-31	C162847	48780-1	9d75b9d0-5122-f424-e053-dadaa90a57ce	Odorono Antiperspirant Deodorant Roll-on Powder

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51048-202-25	OdoronoAntiperspirant and Deodorant Roll-on Powder	74 mL in 1 BOTTLE, WITH APPLICATOR	LIQUID	74		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51048-202	ODORONO ANTIPERSPIRANT AND DEODORANT ROLL-ON POWDER (ALUMINUM CHLOROHYDRATE) LIQUID [OMEGA & DELTA CO]	3	Legacy NDC, 1 package rows	20241121_38d4f89f-01c6-499c-8687-010a0dabc1c8.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
HPN8MZW13M	ALUMINUM CHLOROHYDRATE	12359-72-7	ALUMINUM CHLOROHYDRATE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
51048-202-25	51048020225	74 mL in 1 BOTTLE, WITH APPLICATOR (51048-202-25)	74 ml	2006-05-08	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Odorono Antiperspirant Deodorant Roll-on Powder	Omega & Delta Co	2024-11-19	HUMAN OTC DRUG LABEL	3