Pain Relieving
- Product NDC
- 61010-1560
- 11-digit product format
- 610101560
- Labeler code
- 61010
- Product ID
- 61010-1560_10a94a5e-7097-232e-e063-6294a90a2c98
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- menthol, unspecified form
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Safetec of America, Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-10-07
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 7 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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
- Pain Relieving
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| MENTHOL, UNSPECIFIED FORM | 7 g/100mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| L7T10EIP3A | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1086713 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| df512ce6-ce1b-434d-9571-fb2e1d76e1d0 | Available on FDA.report |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 61010-1560-1 | 2024-02-13 | C162847 | 48780-1 | 1030e365-3fcb-111a-e063-dadaa90a10e2 | 61010-1560-1, Pain Relieving Spray |
| 61010-1560-1 | 2024-01-30 | C162847 | 48780-1 | 1030e365-3fcb-111a-e063-dadaa90a10e2 | 61010-1560-1, Pain Relieving Spray |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 61010-1560-1 | Pain Relieving | 118.3 mL in 1 BOTTLE, SPRAY | SPRAY | 118.3 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 61010-1560 | PAIN RELIEVING (MENTHOL, UNSPECIFIED FORM) SPRAY [SAFETEC OF AMERICA, INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20240214_df512ce6-ce1b-434d-9571-fb2e1d76e1d0.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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Sarna | PRAMOXINE HYDROCHLORIDE | Crown Laboratories | 19b0ce1b-e147-01a1-e063-6394a90af808 | 2026-01-12 | Warnings | M017 |
| Sarna | PRAMOXINE HYDROCHLORIDE, MENTHOL | Crown Laboratories, Inc | 19c41e75-a654-90cf-e063-6394a90a7e97 | 2026-01-12 | Warnings | M017 |
| Itch Relief | DIPHENHYDRAMINE HCL, ZINC ACETATE | HY-VEE, INC | 48350b54-8d9a-48c4-e063-6394a90ac040 | 2026-01-12 | Warnings | M017 |
| LidoPlus Pain Relief | LIDOCAINE HYDROCHLORIDE | Centura Pharmaceuticals, Inc | 07bacc6c-60a6-4297-8663-904a22bdc040 | 2026-01-12 | Warnings | M017 |
| BlueStop Max | EXTERNAL ANALGESIC | Clavel Corporation | f1efb51c-5217-4cb2-e053-2a95a90a7f95 | 2026-01-12 | Warnings | M017 |
| BlueStop Max | EXTERNAL ANALGESIC | Clavel Corporation | f2277e27-868b-57ef-e053-2a95a90abf28 | 2026-01-12 | Warnings | M017 |
| BLT 3 | TETRACAINE | CENTURA PHARMACEUTICALS INC | 401a0d22-1181-02ac-e054-00144ff88e88 | 2026-01-12 | Warnings | M017 |
| Sting Relief Prep Pad | BENZOCAINE | NINGBO TIANBO FIRST AID PRODUCT CO., LTD. | 0c901f64-6890-45c0-9ca7-ee9de87903c4 | 2026-01-12 | Warnings | M017 |
| Goodsense Oral Pain Relief | BENZOCAINE | Geiss, Destin and Dunn, Inc. | eb461b70-d10f-4e11-8374-e43713f3504d | 2026-01-12 | Warnings | M017 |
| Extra Strength Balm | CAPSICUM AND MENTHOL | Saje Natural Business Inc | f516e416-446b-8f21-e053-2a95a90afd88 | 2026-01-12 | Warnings | M017 |
| Pain Release | MENTHOL | Saje Natural Business Inc. | 3df0e56a-7651-42dc-8ed8-f68836a63c61 | 2026-01-12 | Warnings | M017 |
| Trauma Less | MENTHOL | Saje Natural Business Inc. | 650cba4c-6aba-48c3-9c41-841f19905548 | 2026-01-12 | Warnings | M017 |
| Mamisan | LIDOCAINE HYDROCHLORIDE, MENTHOL | Miramar Cosmetics, Inc DBA Miramar Lab | 4402e900-c6e9-4f32-8cc4-c84014384a9f | 2026-01-12 | Warnings | M017 |
| Curist Lidocaine Patch | LIDOCAINE 4% PATCH | Little Pharma, Inc. | 1a8fe44e-7a21-c2ab-e063-6394a90a6100 | 2026-01-11 | Warnings | M017 |
| DG Health Pain Relieving | LIDOCAINE HCL | DOLGENCORP, LLC | 923aeb4c-049f-4ecc-a77e-9ffa0e236d4e | 2026-01-11 | Warnings | M017 |
| Campho-Phenique Antiseptic | CAMPHOR (SYNTHETIC) AND PHENOL | Foundation Consumer Healthcare | 46b84e0b-78a9-4cde-9f90-e165b5419162 | 2026-01-09 | Warnings | M017 |
| MyDerm Pro Freeze Cooling Menthol Pain Relief Roll-On | MENTHOL | Inspec Solutions | 12ff9b9a-73e5-ce31-e063-6294a90aeaf8 | 2026-01-09 | Warnings | M017 |
| Carmex Classic Lip Balm Medicated | CAMPHOR (SYNTHETIC), WHITE PETROLATUM | Carma Laboratories, Inc. | bb0278c9-eaff-d435-e053-2995a90a202a | 2026-01-09 | Warnings | M017 |
| Lidocaine HCI | LIDOCAINE HCI | Trifluent Pharma, LLC | 47f7f06b-720e-eeec-e063-6294a90ae823 | 2026-01-09 | Warnings | M017 |
| Lidocaine | LIDOCAINE | Bellus Medical, LLC | 60cb89f6-e326-0773-e053-2a91aa0a33dd | 2026-01-09 | Warnings | M017 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1086713 | menthol 7 % Topical Spray | PSN | df512ce6-ce1b-434d-9571-fb2e1d76e1d0 | 2 |
| 1086713 | menthol 70 MG/ML Topical Spray | SCD | df512ce6-ce1b-434d-9571-fb2e1d76e1d0 | 2 |
| 1086713 | menthol 7 % Topical Spray | SY | df512ce6-ce1b-434d-9571-fb2e1d76e1d0 | 2 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 61010-1560-1 | 61010156001 | 118.3 mL in 1 BOTTLE, SPRAY (61010-1560-1) | 118.3 ml | 2019-10-07 | 0000-00-00 | No | No | Current |