Blue Star Medicated

Product NDC: 71687-2010
11-digit product format: 716872010
Labeler code: 71687
Product ID: 71687-2010_4feb83a5-9144-0c67-e063-6394a90a710f
Type: HUMAN OTC DRUG
Nonproprietary name: camphor
Dosage form: OINTMENT
Route: TOPICAL
Labeler: Focus Consumer Healthcare, LLC
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2017-10-13
Substance: CAMPHOR (SYNTHETIC)
Active strength: 1.24 g/100g
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

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 · 14 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	71687-2010-2	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	71687-2010-2	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	71687-2010-2	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	71687-2010-2	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	71687-2010-2	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	71687-2010-2	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	71687-2010-2	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

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: Blue Star Medicated
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
CAMPHOR (SYNTHETIC)	1.24 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5TJD82A1ET	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
668306	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
56df008e-a23b-4870-e054-00144ff8d46c	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71687-2010-2	2025-04-01	C162847	48780-1	2cef2736-80ff-d83d-e063-dadaa90ab31f	Blue Star
71687-2010-2	2025-01-30	C162847	48780-1	2cef2736-80ff-d83d-e063-dadaa90ab31f	Blue Star

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71687-2010-2	Blue Star Medicated	56 g in 1 JAR	OINTMENT	56		11
71687-2010-2	Blue Star Medicated	1 in 1 CARTON	OINTMENT	1		11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71687-2010	BLUE STAR MEDICATED (CAMPHOR) OINTMENT [FOCUS CONSUMER HEALTHCARE, LLC]	10	Current NDC, Legacy NDC, 2 package rows	20250416_56df008e-a23b-4870-e054-00144ff8d46c.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 139 of 151 · 3,010 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Bactine Max Bandage	LIDOCAINE	WellSpring Pharmaceutical Corporation	465dc46e-6435-4569-9516-f648d0fe0f09	2023-12-21	Warnings	Exact identifier application number: M017
Valtrum IMMEDIATE ACTION TOPICAL ANALGESIC	CAMPHOR, MENTHOL, METHYL SALICYLATE	LABORATORIOS QUANTIUM LLC	c4efa317-8dd1-49e1-b7ca-9df2147edd3e	2023-12-21	Warnings	Exact identifier application number: M017
DDM Camphor Spirit	CAMPHOR 10%	Discount Drug Mart	5d56cbe6-4e48-79eb-e053-2a91aa0a74d3	2023-12-20	Warnings	Exact identifier application number: M017
Quality Choice Camphor Spirit	CAMPHOR 10%	Chain Drug Market Association	8d352a67-2024-43d0-b525-038d398949e6	2023-12-20	Warnings	Exact identifier application number: M017
Instant Antiseptic Pain Relief	CAMPHOR 10.8% AND PHENOL 4.7%	Chain Drug Market Association	2cd60df3-bfde-4747-ba4f-7121612f2e63	2023-12-20	Warnings	Exact identifier application number: M017
Poison Ivy Wash	PRAMOXINE HCL	Chain Drug Market Association	873a546b-90ae-50cb-e053-2a91aa0adbfb	2023-12-20	Warnings	Exact identifier application number: M017
Premier Value Instant Antiseptic Pain Relief	CAMPHOR 10.8% AND PHENOL 4.7%	Pharmacy Value Alliance LLC	9d63f8ed-fc50-0d84-e053-2a95a90a6e92	2023-12-20	Warnings	Exact identifier application number: M017
Ear Drops	CARBAMIDE PEROXIDE 6.5%	CVS Pharmacy	8a872991-01af-5fd0-e053-2995a90ac7f4	2023-12-20	Warnings	Exact identifier application number: M017
CVS Cold and Hot Roll-On	COOL AND HEAT PAIN RELIEF	CVS Pharmacy	b8cc578a-be6d-90c0-e053-2995a90a7742	2023-12-20	Warnings	Exact identifier application number: M017
Sunmark Camphor Spirit	CAMPHOR 10%	Strategic Sourcing Services LLC	667b3a9f-4a5c-4ef0-adbd-cce9a5f94faa	2023-12-19	Warnings	Exact identifier application number: M017
DDM Instant Antiseptic Pain Relief	CAMPHOR 10.8% AND PHENOL 4.7%	Discount Drug Mart	5d56c74f-604d-4fed-e053-2a91aa0a417c	2023-12-19	Warnings	Exact identifier application number: M017
HEB Camphor Phenol	CAMPHOR 10.8% AND PHENOL 4.7%	H E B	5d573883-001d-e5a4-e053-2991aa0a6203	2023-12-18	Warnings	Exact identifier application number: M017
Petrocort Antipruritic Lip 21	HYDROCORTISONE	Clinical Formula LLC	7d408e08-d777-4dfb-bb5e-b4fe5d6f4c7b	2023-12-15	Warnings	Exact identifier application number: M017
DermaWound Wound Care Venous Stasis	BENZOCAINE HYDROCHLORIDE	Progressive Doctors, LLC	6221ba86-8b7f-48c8-8284-6950f9fc36b1	2023-12-15	Warnings	Exact identifier application number: M017
Lidocaine Pain Relief Roll-On	LIDOCAINE 4%	Humco Holding Group, Inc.	a8be9e46-1616-40a9-e053-2a95a90ac3bc	2023-12-15	Warnings	Exact identifier application number: M017
Hot/Cold Menthol 16% Roll-On	HOT/COLD MENTHOL 16% ROLL-ON	Humco Holding Group, Inc	a8bf9744-9979-13c1-e053-2a95a90a30aa	2023-12-15	Warnings	Exact identifier application number: M017
Freds Medicated anti itch	PRAMOXINE HYDROCHLORIDE, MENTHOL	Discount Drug Mart	8697b932-da5a-717e-e053-2a91aa0afcae	2023-12-12	Warnings	Exact identifier application number: M017
CVS Medicated anti itch	PRAMOXINE HYDROCHLORIDE, MENTHOL	CVS	86972218-31fe-6942-e053-2991aa0a8850	2023-12-12	Warnings	Exact identifier application number: M017
Best Choice Medicated anti itch	PRAMOXINE HYDROCHLORIDE, MENTHOL	value merchandisers	869631f8-aa1e-8ea4-e053-2a91aa0a5c57	2023-12-12	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE 1%	Weeks & Leo Co., Inc.	0c5325e3-4796-856c-e063-6394a90a1f90	2023-12-12	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5TJD82A1ET	CAMPHOR (SYNTHETIC)	76-22-2	CAMPHOR (SYNTHETIC)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
668306	camphor 1.24 % Topical Ointment	PSN	56df008e-a23b-4870-e054-00144ff8d46c	11
668306	camphor 0.0124 MG/MG Topical Ointment	SCD	56df008e-a23b-4870-e054-00144ff8d46c	11
668306	camphor 1.24 % Topical Ointment	SY	56df008e-a23b-4870-e054-00144ff8d46c	11

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
71687-2010-2	71687201002	1 JAR in 1 CARTON (71687-2010-2) / 56 g in 1 JAR	1 jar	2017-12-11	0000-00-00	No	No	Current