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 |
|---|---|---|---|---|---|---|
| HAWAIIAN TROPIC | AVOBENZONE, HOMOSALATE, OCTOCRYLENE | Edgewell Personal Care Brands LLC | 5990fe66-4fa2-06aa-e063-6294a90a5261 | 2026-08-21 | Warnings | M020 |
| Hawaiian Tropic | AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE | Edgewell Personal Care Brands LLC | 5991466a-e729-16b7-e063-6394a90a11ff | 2026-08-21 | Warnings | M020 |
| Avobenzone, Homosalate, Octisalate | AVOBENZONE, HOMOSALATE, OCTISALATE | Topco Associates LLC | 597b78df-83cb-1b21-e063-6294a90a56a8 | 2026-08-20 | Warnings, Adverse reactions | M020 |
| Sunski Base Camp Face and Body Sunscreen SPF 45 | HOMOSALATE, OCTISALATE, AVOBENZONE | Stewart Charley Ventures, LLC | 2fc45f85-a6f8-4893-8b34-4db5e39cb615 | 2026-08-20 | Warnings | M020 |
| Sweat Resistant Sunscreen Body Original | TITANIUM DIOXIDE, ZINC OXIDE | Clutch, Inc. | 4bbde755-e312-123e-e063-6294a90a467f | 2026-08-20 | Warnings | M020 |
| Sunscreen | BROAD SPECTRUM SPF 30 | Concierge Choice LLC | 5980055b-493e-4763-e063-6294a90a570f | 2026-08-20 | Warnings | M020 |
| Lip Balm SPF 15 | AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE | Skin Script, LLC | 20c5fde7-ee8f-4b74-e063-6394a90a93ec | 2026-08-19 | Warnings | M020 |
| Aloe UP .5OZ SPF 50 MINERAL Sunscreen | ZINC OXIDE 14.69% | Aloe Care International, LLC | 6ad80af3-78cd-4211-a5f2-68531aae264a | 2026-08-19 | Warnings | M020 |
| Utu Broad Spectrum SPF 50 Tinted Sunscreen-Stick | ZINC OXIDE | Utu Co | 596e17d3-3064-1cda-e063-6294a90af963 | 2026-08-19 | Warnings | M020 |
| Mineral sunscreen | MINERAL SUNSCREEN | Guangzhou Origin Beauty Cosmetics Co., Ltd. | 59713657-a7ef-1aee-e063-6394a90a326e | 2026-08-19 | Warnings | M020 |
| The Naked Bee SPF 50 Mineral Sunscreen | ZINC OXIDE 14.69% | The Naked Bee | f820a9be-c94d-4fd5-b202-2dda5746a82a | 2026-08-18 | Warnings | M020 |
| The Naked Bee SPF 50 Mineral Sunscreen | ZINC OXIDE 20% | The Naked Bee | 7dd2b1cd-e229-4eeb-8122-46fde5af1091 | 2026-08-18 | Warnings | M020 |
| Sun Zapper - Baby pure zinc sunscreen SPF30 | ZINC OXIDE SUNSCREEN | VEGANIC SKN LIMITED | 3ee52faa-64a8-4bdf-e063-6294a90a65cf | 2026-08-17 | Warnings | M020 |
| Sun Zapper - Face pure zinc sunscreen SPF30 | ZINC OXIDE SUNSCREEN | VEGANIC SKN LIMITED | 3ee4feb3-6966-67f9-e063-6394a90a16d5 | 2026-08-17 | Warnings | M020 |
| HEADHUNTER SURF SCREEN SPF 50 SUNSCREEN | ZINC OXIDE,TITANIUM DIOXIDE | Guangzhou Tata Biotechnology Co., Ltd. | 4339df13-77d3-31a1-e063-6394a90a5208 | 2026-08-17 | Warnings | M020 |
| Soleil Defense Sunscreen | BROAD SPECTRUM SPF 30 | AMARA MED SPA LLC | 594244b1-db3b-002b-e063-6394a90a0329 | 2026-08-17 | Warnings | M020 |
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | HAMBLIN DERMATOLOGY | 5942e64c-416e-7525-e063-6394a90a2839 | 2026-08-17 | Warnings | M020 |
| Protect Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | Opal Day Spa | 5943413a-48e1-0bdf-e063-6294a90a2fff | 2026-08-17 | Warnings | M020 |
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | MedSpa By Beauty Bar LLC | 5943ba3d-688e-9e9c-e063-6294a90afa9a | 2026-08-17 | Warnings | M020 |
| Sunscreen | BROAD SPECTRUM SPF 30 | Charleston Dermatology, P.C. | 59440f7f-4213-6e2b-e063-6394a90af483 | 2026-08-17 | 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 |