DCH Pain Relief Roll-On

Product NDC: 72839-087
11-digit product format: 728390087
Labeler code: 72839
Product ID: 72839-087_29a4c95d-6ce1-955f-e063-6294a90a1846
Type: HUMAN OTC DRUG
Nonproprietary name: Lidocaine HCl 4%
Dosage form: GEL
Route: TOPICAL
Labeler: Derma Care Research Labs, LLC
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2022-04-21
Substance: LIDOCAINE HYDROCHLORIDE
Active strength: 4 g/100g
Pharmacologic classes: Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag: No
Listing certified through: 2026-12-31
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: DCH Pain Relief Roll-On
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
LIDOCAINE HYDROCHLORIDE	4 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
V13007Z41A	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1010077	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
fda35d37-f36e-efc8-e053-6294a90a2bb8	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
860a93dc-4863-49cc-b284-6bbe8191bc48	Product name	4	20250214
eaba870a-6a9d-442e-8643-87b3f558a451	Product name	1	20250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86	Product name	1	20230117
fa8b5901-e681-426f-82fe-54f6d81ec698	Product name	4	20180619
332d03e4-aa24-4b11-841a-02bf41081920	Product name	1	20171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070	Product name	1	20171221
68ed98f8-24c2-44a0-944a-6d36e82ce25a	Product name	1	20141222
1cd42bc2-a430-c72b-636d-991b235fbf80	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72839-087-02	DCH Pain Relief Roll-On	1 in 1 CARTON	GEL	1		2
72839-087-02	DCH Pain Relief Roll-On	71 g in 1 BOTTLE	GEL	71		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72839-087	DCH PAIN RELIEF ROLL-ON (LIDOCAINE HCL 4%) GEL [DERMA CARE RESEARCH LABS, LLC]	2	Current NDC, 2 package rows	20241222_fda35d37-f36e-efc8-e053-6294a90a2bb8.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 65 of 354 · 7,077 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SHISEIDO URBAN ENVIRONMENT VITA-CLEAR SUNSCREEN	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	SHISEIDO AMERICAS CORPORATION	60e55ebb-47b8-465e-819a-af195952e1ca	2026-02-04	Warnings	Exact identifier application number: M020
SHISEIDO BENEFIANCE NUTRIPERFECT DAY	AVOBENZONE, OCTINOXATE, AND OCTOCRYLENE	SHISEIDO AMERICAS CORPORATION	f644c67b-3a71-411b-b321-39a8b18af0c7	2026-02-04	Warnings	Exact identifier application number: M020
cle de peau BEAUTE UV PROTECTIVE N	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Shiseido Americas Corporation	4b242b76-8aed-4939-9906-741828acd815	2026-02-04	Warnings	Exact identifier application number: M020
cle de peau BEAUTE PORE-REFINING MATTIFYING VEIL	AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE	Shiseido Americas Corporation	efcf240f-95cb-45e0-b58a-9c8f3609aa55	2026-02-04	Warnings	Exact identifier application number: M020
cle de peau BEAUTE PORE-REFINING MATTIFYING VEIL	AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE	Shiseido Americas Corporation	270ecc83-4262-4102-a753-2acaf11360a0	2026-02-04	Warnings	Exact identifier application number: M020
Walgreens 50 Caramel and Pistachio Scented Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	WALGREEN COMPANY	4a038017-9f15-b4b2-e063-6294a90a1b23	2026-02-04	Warnings	Exact identifier application number: M020
SHISEIDO ULTIMATE SUN PROTECTOR	OCTISALATE, OCTOCRYLENE, ZINC OXIDE	Shiseido Americas Corporation	ce6a28c1-56e6-4105-bc9d-9d1986ead420	2026-02-04	Warnings	Exact identifier application number: M020
Sport Sunscreen SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE	HARRIS TEETER	d52e2c61-edbc-4c26-b1a7-e8eb656db188	2026-02-04	Warnings, Adverse reactions	Exact identifier application number: M020
Sport Sunscreen SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE	HARRIS TEETER	d365ed6d-a92f-473b-be19-b8b63d17f3b7	2026-02-04	Warnings, Adverse reactions	Exact identifier application number: M020
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	HARRIS TEETER	0a3b4597-06fe-4689-9751-6577867d755e	2026-02-04	Warnings, Adverse reactions	Exact identifier application number: M020
Sport Sunscreen SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE	HARRIS TEETER	b83ea476-fa32-4405-9ae3-f294836edb62	2026-02-04	Warnings	Exact identifier application number: M020
Sunplus SPF50 Face Body Sunscreen	SUNSCREEN	I.Shay Cosmetics	26d55baf-66dc-b1b8-e063-6394a90a670d	2026-02-04	Warnings	Exact identifier application number: M020
NUDESCREEN DEWY ILLUMINATING GLOW SPF 30 - Angel Glow	ZINC OXIDE SUNSCREEN	Bentley Laboratories, LLC	351217c4-8d71-41d9-ab08-c43857c0510c	2026-02-04	Warnings	Exact identifier application number: M020
NIDA Invisible Fit Sun Stick	SUN STICK	Proso Corp	49eca4f2-aae3-a0d5-e063-6394a90ab25f	2026-02-03	Warnings	Exact identifier application number: M020
Shiny Hiny SPF 45 Mineral Sunscreen	ZINC OXIDE	Shiny Hiny Products, LLC	31adde36-5e1b-40ff-e063-6294a90a6f2e	2026-02-03	Warnings	Exact identifier application number: M020
Walgreens 50 Passion Fruit Scented Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	WALGREEN COMPANY	49f030d8-959c-a3cd-e063-6294a90ae1ba	2026-02-03	Warnings	Exact identifier application number: M020
Zealios Mineral SPF 30 Sunscreen	ZINC OXIDE	Personal Best Products Inc. dba Zealios	c421b00c-6536-4455-81f6-01686f8c2388	2026-02-03	Warnings	Exact identifier application number: M020
Zealios Sport Performance Ultralight SPF 50 Sunscreen	HOMOSALATE, OCTOCRYLENE, OCTISALATE, AND AVOBENZONE	Personal Best Products Inc. dba Zealios	020bd1b4-da50-4117-a4f3-b74aa4187396	2026-02-03	Warnings	Exact identifier application number: M020
Adrien Arpel Daily Defense Moisturizer SPF 30	AVOBENZONE, OCTISALATE, OCTOCRYLENE	Color Me Beautiful Inc	f65e1428-b79a-4126-862a-907ca17ee8f7	2026-02-02	Warnings	Exact identifier application number: M020
Flori Roberts Daily Defense Moisturizer SPF 30	AVOBENZONE, OCTISALATE, OCTOCRYLENE	Color Me Beautiful Inc	934d6b80-0cc3-4dcd-a25d-2191bd273618	2026-02-02	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
V13007Z41A	LIDOCAINE HYDROCHLORIDE	6108-05-0	LIDOCAINE HYDROCHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1010077	lidocaine HCl 4 % Topical Gel	PSN	fda35d37-f36e-efc8-e053-6294a90a2bb8	2
1010077	lidocaine hydrochloride 0.04 MG/MG Topical Gel	SCD	fda35d37-f36e-efc8-e053-6294a90a2bb8	2
1010077	lidocaine hydrochloride 4 % Topical Gel	SY	fda35d37-f36e-efc8-e053-6294a90a2bb8	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
72839-087-02	72839008702	1 BOTTLE in 1 CARTON (72839-087-02) / 71 g in 1 BOTTLE	1 bottle	2022-04-21	No	No	Current