Sarna

Product NDC: 0316-0230
11-digit product format: 003160230
Labeler code: 0316
Product ID: 0316-0230_48341fc1-10ea-47fa-e063-6394a90abe32
Type: HUMAN OTC DRUG
Nonproprietary name: Pramoxine Hydrochloride
Dosage form: LOTION
Route: TOPICAL
Labeler: Crown Laboratories
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2024-01-01
Substance: PRAMOXINE HYDROCHLORIDE
Active strength: 10 mg/mL
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	0316-0230		D	Discontinued by firm		2026-10-23
excluded package	package	0316-0230	0316-0230-75	D	Discontinued by firm		2026-10-23

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 · 2 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
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product	0316-0230		D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	0316-0230	0316-0230-75	D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`

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: Sarna
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
PRAMOXINE HYDROCHLORIDE	10 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
88AYB867L5	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1246075	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
19b0ce1b-e147-01a1-e063-6394a90af808	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
58f3f9b7-3b9b-a9c1-1c9f-18ac777192b8	Product name	1	20140508
9869efd7-d6dd-0665-5b67-53adbe6ef15e	Product name	1	20140508
a7051cba-790b-a699-81f8-dbbbdbd9b5ac	Product name	1	20140508
da108d9e-edc8-17a3-8c28-3251c6a8accc	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0316-0230-75	2023-02-13	C162847	48780-1	f386c64a-0288-0266-e053-dadaa90a7c1a	Sarna Sensitive
0316-0230-75	2023-01-30	C162847	48780-1	f386c64a-0288-0266-e053-dadaa90a7c1a	Sarna Sensitive

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0316-0230-12	Sarna	355 mL in 1 BOTTLE, PUMP	LOTION	355	5
0316-0230-25	Sarna	5 mL in 1 PACKET	LOTION	5	5
0316-0230-57	Sarna	222 mL in 1 BOTTLE, PUMP	LOTION	222	5

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0316-0230-75	ML - Milliliter	0316-0230	c47fd8d6-cdae-4078-8f6f-5cdc699dcd3b	1	2019-01-24

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0316-0230	SARNA (PRAMOXINE HYDROCHLORIDE) LOTION [CROWN LABORATORIES]	20	Current NDC, Legacy NDC	20240602_7b2ff573-ca59-d69a-e053-2a91aa0abcec.zip
0316-0230	SARNA (PRAMOXINE HYDROCHLORIDE) LOTION [CROWN LABORATORIES]	2	Current NDC, Legacy NDC, 3 package rows	20250323_19b0ce1b-e147-01a1-e063-6394a90af808.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 17 of 151 · 3,020 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MyDerm Aloe and Lidocaine	LIDOCAINE	Medline Industries	fdfd4388-cd27-467b-959b-249a49ea5cf6	2026-05-26	Warnings	Exact identifier application number: M017
MyDerm Aloe and Lidocaine	LIDOCAINE	Inspec Solutions LLC.	4939c663-a876-4527-822a-df02964fa694	2026-05-26	Warnings	Exact identifier application number: M017
Lidocaine Menthol Pain Relief	LIDOCAINE, MENTHOL	Amerisource Bergen	94039190-dde3-4d8e-873a-79abd3f6208b	2026-05-26	Warnings	Exact identifier application number: M017
topcare hydrocortisone	HYDROCORTISONE	Topco Associates LLC	858053a0-d888-4bb9-b94e-503bcf3864cb	2026-05-21	Warnings	Exact identifier application number: M017
Arthritis Pain Relief Cream	HISTAMINE DIHYDROCHLORIDE	Sombra Cosmetics Inc.	523333ee-eccd-bcf7-e063-6394a90aea60	2026-05-21	Warnings	Exact identifier application number: M017
North Star Nutritionals Soothanol X3 Pain Relieving Drops	MENTHOL	NEWMARKET HEALTH PRODUCTS, LLC	068343b8-0435-40d0-846c-9d8624e8b6c4	2026-05-21	Warnings	Exact identifier application number: M017
DO ME DELAY	LIDOCAINE HCL	Prodigy Media Inc	5255ee85-6f29-0776-e063-6394a90a525b	2026-05-21	Warnings	Exact identifier application number: M017
Australian Dream Back Pain	HISTAMINE DIHYDROCHLORIDE	Sombra Cosmetics Inc.	5256a63e-e6da-84c1-e063-6294a90a8dff	2026-05-21	Warnings	Exact identifier application number: M017
SINSIN HANBANG FLEX	CAMPHOR, MENTHOL	Sinsin Pharmaceutical co., ltd.	525c5d18-bfc1-3002-e063-6394a90a5b1d	2026-05-21	Warnings	Exact identifier application number: M017
LidoPro Patch	LIDOCAINE, MENTHOL, AND METHYL SALICYLATE	Preferred Pharmaceuticals Inc.	6c9a076e-6316-427b-9ce6-c8fe2d388837	2026-05-21	Warnings	Exact identifier application number: M017
Medi-First Capsaicin Cream	CAPSAICIN	Unifirst First Aid Corporation	49eb807b-fa31-3d84-e063-6394a90acfcf	2026-05-20	Warnings	Exact identifier application number: M017
Biofreeze Triple Target Roll-On	CAMPHOR, CAPSAICIN, MENTHOL	Reckitt Benckiser LLC	5089c088-3026-233a-e063-6394a90a93b6	2026-05-19	Warnings	Exact identifier application number: M017
Lidocaine Pain Relief Patch	LIDOCAINE	GERI-CARE PHARMACEUTICAL CORP	522f1521-f9f2-4c26-e063-6394a90a9e05	2026-05-19	Warnings	Exact identifier application number: M017
Easment 0.1% Capsaicin Roll on	CAPSAICIN 0.1%	Easment LLC	521212d6-57fd-4a7a-e063-6294a90a2a18	2026-05-18	Warnings	Exact identifier application number: M017
Burn Relief	LIDOCAINE	WALMART INC.	15af4557-4baf-c177-e063-6294a90a7a5b	2026-05-18	Warnings	Exact identifier application number: M017
Blistex Maximum Hydration Lip	CAMPHOR (SYNTHETIC), DIMETHICONE, UNSPECIFIED, MENTHOL, UNSPECIFIED FORM, AND PHENOL	Blistex Inc.	fed223bc-edf3-46eb-b678-acb906f9ef11	2026-05-18	Warnings	Exact identifier application number: M017
Tiger Balm	CAMPHOR (SYNTHETIC), MENTHOL, AND CAPSICUM	Haw Par Healthcare Ltd.	5066dc10-e4d5-49e9-9a5f-0ac220cfbf28	2026-05-18	Warnings	Exact identifier application number: M017
Deep Blue Mini	MENTHOL	doTERRA International, LLC	51dd58a8-1fd5-9cd7-e063-6394a90a1f72	2026-05-15	Warnings	Exact identifier application number: M017
Biofreeze Overnight Gel	MENTHOL	Reckitt Benckiser LLC	f5c8c08b-c7c0-f84d-e053-2a95a90add15	2026-05-15	Warnings	Exact identifier application number: M017
Biofreeze Professional	MENTHOL, UNSPECIFIED FORM	Reckitt Benckiser LLC	00bba5d2-b0e0-701c-e063-6294a90a5741	2026-05-15	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
88AYB867L5	PRAMOXINE HYDROCHLORIDE	637-58-1	PRAMOXINE HYDROCHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1246075	pramoxine HCl 1 % Topical Lotion	PSN	19b0ce1b-e147-01a1-e063-6394a90af808	5
1246075	pramoxine hydrochloride 10 MG/ML Topical Lotion	SCD	19b0ce1b-e147-01a1-e063-6394a90af808	5
1246075	pramoxine hydrochloride 1 % Topical Lotion	SY	19b0ce1b-e147-01a1-e063-6394a90af808	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0316-0230-12	00316023012	355 mL in 1 BOTTLE, PUMP (0316-0230-12)	355 ml	2024-01-01		No	No	Current
0316-0230-25	00316023025	5 mL in 1 PACKET (0316-0230-25)	5 ml	2024-03-18		Yes	No	Current
0316-0230-57	00316023057	222 mL in 1 BOTTLE, PUMP (0316-0230-57)	222 ml	2024-01-01		No	No	Current
0316-0230-75	00316023075	222 mL in 1 BOTTLE, PUMP (0316-0230-75)	222 ml	2018-12-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Sarna Sensitive	Crown Laboratories \| Crown Laboratories, Inc.	2026-01-12	HUMAN OTC DRUG LABEL	5
Sarna Sensitive	Crown Laboratories \| Crown Laboratories, Inc.	2024-05-31	HUMAN OTC DRUG LABEL	20