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 73 of 353 · 7,049 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer Shade Five	ZINC OXIDE	Clean Beauty For All, Inc (dba Saie)	39ae4a97-7f96-4c95-a6de-0c779764fb02	2026-01-20	Warnings	Exact identifier application number: M020
Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer Shade Four and Half	ZINC OXIDE	Clean Beauty For All, Inc (dba Saie)	1922fc3e-055c-e51d-e063-6294a90a00f5	2026-01-20	Warnings	Exact identifier application number: M020
Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer Shade Nine	ZINC OXIDE	Clean Beauty For All, Inc (dba Saie)	9c7a31df-5bdd-403b-b807-1d1a801e1bb6	2026-01-20	Warnings	Exact identifier application number: M020
Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer Shade One	ZINC OXIDE	Clean Beauty For All, Inc (dba Saie)	1922fc51-ae53-acb8-e063-6394a90a14eb	2026-01-20	Warnings	Exact identifier application number: M020
Wrinkle Repair Moisturizer SPF 30 EQB	AVOBENZONE 2% HOMOSALATE 4% OCTISALATE 4% OCTOCRYLENE 2%	Walmart	a067e968-e598-40ef-95f2-c338b5e413dd	2026-01-20	Warnings	Exact identifier application number: M020
Welmedix HomeCare PRO Fragile Skin Dual Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Welmedix LLC	48da4589-0f5a-c25b-e063-6394a90ac18b	2026-01-20	Warnings	Exact identifier application number: M020
SPF 50 Mineral Sunscreen Kids	ZINC OXIDE 14.69%	S&C Hampton Sun LLC	0bdb7d15-dc52-4e23-9417-fe73f17f6110	2026-01-20	Warnings	Exact identifier application number: M020
DEWYTREE URBAN SHADE INVISIBLE SMOOTHING PORE SUNSTIC SUNSTICK	OCTOCRYLENE, HOMOSALATE, ZINC OXIDE, OCTISALATE	DEWYTREE CO. ,LTD	48406e68-eefd-d2c2-e063-6394a90a4ad9	2026-01-20	Warnings	Exact identifier application number: M020
KONEUK SUNSCREEN SPF50	KONEUK SUNSCREEN SPF50	Guangzhou Meixi Biotechnology Co., Ltd.	48dd7f6e-2a4d-2c92-e063-6294a90a4255	2026-01-20	Warnings	Exact identifier application number: M020
CHUDA	AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE	Premier Ocher LLC	1bc2a2df-a4cd-45e7-93c6-b35dbd8b280f	2026-01-20	Warnings	Exact identifier application number: M020
Dior Forever Skin Glow Flawless Radiant Skin True Foundation SPF 25 2CR Cool Fosy	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	12edec55-2414-4bbd-bc96-4599a96b96ac	2026-01-19	Warnings	Exact identifier application number: M020
PROJECT REEF SPF-30 Mineral Sunscreen	ZINC OXIDE	Project Reef LLC	a6077e6f-d987-4159-946f-3e2397247659	2026-01-19	Warnings	Exact identifier application number: M020
OUTER REEF MINERAL SUNSCREEN SPF 30	TITANIUM DIOXIDE	Coral Reef Park Co., Inc.	86ee2fdf-8a88-44e6-b12a-36a92360477a	2026-01-19	Warnings	Exact identifier application number: M020
SABAL Mineral Sunscreen Broad Sprectrum SPF 30	ZINC OXIDE	SABAL SUN LLC	f917b446-4e10-4231-826e-fdac32e11186	2026-01-19	Warnings	Exact identifier application number: M020
Plius Daily SPF Moisturizer SPF 30	AVOBENZONE, OCTISALATE, OCTOCRYLENE	PLIUS, Inc	31866de9-afa0-4c11-be65-b61373551493	2026-01-19	Warnings	Exact identifier application number: M020
PROTEKT SPF-50 Sheer Mineral Sunscreen	ZINC OXIDE	Protekt Products, Inc.	6edc0941-bb21-4797-a875-81f727694774	2026-01-19	Warnings	Exact identifier application number: M020
Ultra Violette SPF Mini Mates Duo Pocket Pals Ultra Violette SPF Mini Mates Duo Pocket Pals Contains 1 X Supreme Screen SPF50 20mL (84803-100-21) 1 X Future Screen SPF50 20mL (84803-103-21)	ACTIVE INGREDIENTS SUPREME SCREEN SPF 50 AVOBENZONE 3% HOMOSALATE 7% OCTISALATE 5% OCTOCRYLENE 8% ACTIVE INGREDIENTS FUTURE SCREEN SPF 50 ZINC OXIDE 20%	Grace and Fire USA Inc.	48c1b93c-9c6f-95aa-e063-6294a90a0cfa	2026-01-19	Warnings	Exact identifier application number: M020
ANUA INVISIBLE GLOW FINISH SUNSCREEN	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	The Founders Inc.	446ac344-1078-4cd1-e063-6294a90a4bd4	2026-01-19	Warnings	Exact identifier application number: M020
ANUA ZERO-CAST MOISTURIZING FINISH SUNSCREEN	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	The Founders Inc.	31af7b5e-2bd6-63ee-e063-6294a90a0806	2026-01-19	Warnings	Exact identifier application number: M020
ANUA INVISIBLE MATTE FINISH SUNSCREEN	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	The Founders Inc.	4248deaf-ad55-a9b4-e063-6294a90a55cc	2026-01-19	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