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 |
|---|---|
| LIDOCAINE HYDROCHLORIDE | 4 g/100g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| V13007Z41A | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1010077 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| fda35d37-f36e-efc8-e053-6294a90a2bb8 | Available on FDA.report |
DailyMed Product Concepts#
| 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 | 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#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Unseen Sunscreen Body SPF 40 | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | Supergoop, LLC | ec1c30bd-76e1-9d00-e053-2a95a90a1759 | 2026-01-09 | Warnings | M020 |
| Glow Screen SPF 40 | AVOBENZONE, OCTISALATE, OCTOCYLENE | Supergoop, LLC | 21569637-332a-461b-bf6c-33af6a83a155 | 2026-01-09 | Warnings | M020 |
| Glowscreen SPF 40 - Dawn | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | Supergoop, LLC | f07145d5-b74d-7757-e053-2a95a90ac4c0 | 2026-01-09 | Warnings | M020 |
| Glowscreen SPF 40 -Sunset | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | Supergoop, LLC | f7e493da-8fc6-191d-e053-6294a90aa483 | 2026-01-09 | Warnings | M020 |
| Supergoop Glow Screen SPF 40 Shade 2 Golden Hour | BROAD SPECTRUM SUNSCREEN | Supergoop LLC | d2928dd7-a813-4929-e053-2a95a90aaeb4 | 2026-01-09 | Warnings | M020 |
| Superscreen Hydrating Daily Cream SPF 40 | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | Supergoop, LLC | ff0e4e97-8f01-bd36-e053-6394a90a47ae | 2026-01-09 | Warnings | M020 |
| Lipshade SPF 30 Hey Yall | ZINC OXIDE | Supergoop, LLC | f93dfa13-ff18-ee38-e053-6394a90aea46 | 2026-01-09 | Warnings | M020 |
| Triple Prep SPF 40 | AVOBENZONE, OCTISALATE, OCTOCRYLENE, HOMOSALATE | Supergoop, LLC | 004df4e5-dba9-6030-e063-6394a90a76d3 | 2026-01-09 | Warnings | M020 |
| Unseen Sunscreen Lip Protector SPF 30 | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | Supergoop, LLC | 12605fb4-0de6-94f3-e063-6294a90a3a6f | 2026-01-09 | Warnings | M020 |
| Unseen Sunscreen Stick SPF 40 | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | Supergoop, LLC | 2735c5c7-a4ef-33c3-e063-6294a90abf97 | 2026-01-09 | Warnings | M020 |
| PLAY Sunscreen SPF 50 | HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE | Supergoop LLC | 2860d42c-d644-8b5a-e063-6394a90aec10 | 2026-01-09 | Warnings | M020 |
| PLAY Mineral SPF 30 with Green Algae | ZINC OXIDE | Supergoop LLC | 29a1ff4b-3875-5275-e063-6394a90a53fd | 2026-01-09 | Warnings | M020 |
| Every. Single. Face. Watery SPF 50 | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | Supergoop, LLC | d086a9b8-19e5-f713-e053-2995a90aa976 | 2026-01-09 | Warnings | M020 |
| 3D Tinted Moisturizing BS SPF 30 | ZINC OXIDE | Allure Labs | 47fd415f-819e-bbb8-e063-6394a90a2c6a | 2026-01-09 | Warnings | M020 |
| ST MORIZ SUNCARE BODY SUNSCREEN SPF50 | SUNCARE BODY SUNSCREEN SPF50 | Aopline Biotechnology (Guangzhou) Co., Ltd. | 4801cfd2-1fe2-d118-e063-6294a90a6c8b | 2026-01-09 | Warnings | M020 |
| ST MORIZ SUNCARE BODY SUNSCREEN SPF30 | SUNCARE BODY SUNSCREEN SPF30 | Aopline Biotechnology (Guangzhou) Co., Ltd. | 48026f09-6d15-8fa6-e063-6294a90a17cb | 2026-01-09 | Warnings | M020 |
| RODAN and FIELDS ENHANCEMENTS MEDIUM | TITANIUM DIOXIDE, ZINC OXIDE | Bentley Laboratories, LLC | 6aa6ad3f-2c52-4031-9e6c-7526c42de71d | 2026-01-09 | Warnings | M020 |
| FACE SPF 47 SETTING | FACE SPF 47 SETTING SPRAY | Aopline Biotechnology (Guangzhou) Co., Ltd. | 47db9a54-c02f-d2ea-e063-6394a90ab973 | 2026-01-08 | Warnings | M020 |
| BADABOOM SUNSCREEN | SUNSCREEN | Aopline Biotechnology (Guangzhou) Co., Ltd. | 47dbf363-2892-4530-e063-6294a90abe1f | 2026-01-08 | Warnings | M020 |
| ROE WELLNESS SPF 50 MINERAL | SPF 50 MINERAL POWDER | Aopline Biotechnology (Guangzhou) Co., Ltd. | 47dc8155-4abb-4bb7-e063-6294a90af1ad | 2026-01-08 | Warnings | M020 |
DailyMed RxNorm Mappings#
| 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 | 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 |