NOVUM
- Product NDC
- 69574-005
- 11-digit product format
- 695740005
- Labeler code
- 69574
- Product ID
- 69574-005_32322747-0600-c81a-e063-6394a90ac71e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- menthol
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- NOVUM SOLUTIONS INC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2015-05-19
- Substance
- MENTHOL
- Active strength
- .5 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Package NDC | Code | Status | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded product | product | I | Inactivated by FDA | 2ef7874e63bc… | 57b86245f4fa… | |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded package | package | 69574-005-05 | I | Inactivated by FDA | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded product | product | I | Inactivated by FDA | a1b67e2a42f9… | c4cf2c586c0d… | |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded package | package | 69574-005-05 | I | Inactivated by FDA | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded product | product | I | Inactivated by FDA | cfe11265f3b6… | 090c488252e2… | |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded package | package | 69574-005-05 | I | Inactivated by FDA | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded product | product | I | Inactivated by FDA | cdf11ea48f46… | ba0047e9e063… | |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded package | package | 69574-005-05 | I | Inactivated by FDA | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded product | product | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… | |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 69574-005-05 | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded product | product | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… | |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 69574-005-05 | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded product | product | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… | |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 69574-005-05 | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… |
| 2019-12-08 06:16 UTC · source 2019-12-05 | excluded product | product | E | Excluded after deficient or non-compliant submission was not corrected | 110d247fa046… | a55b01930146… | |
| 2019-12-08 06:16 UTC · source 2019-12-05 | excluded package | package | 69574-005-05 | E | Excluded after deficient or non-compliant submission was not corrected | 110d247fa046… | a55b01930146… |
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
- NOVUM
- Brand name suffix
- APR
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| MENTHOL | .5 g/100mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| L7T10EIP3A | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1314935 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1b869a1f-5787-4d03-a546-43a8217b2b2c | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 6c13b22c-b3ba-4127-b768-0132dd5ab0d1 | Product name | 1 | 20230829 |
FDA-Initiated Inactive NDC Indexing#
| Effective | Related label |
|---|---|
| 2025-04-07 | 1b869a1f-5787-4d03-a546-43a8217b2b2c |
| 2025-01-30 | 1b869a1f-5787-4d03-a546-43a8217b2b2c |
| 2023-11-03 | 1b869a1f-5787-4d03-a546-43a8217b2b2c |
| 2023-01-30 | 1b869a1f-5787-4d03-a546-43a8217b2b2c |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69574-005-04 | NOVUMAPR | 118.3 mL in 1 BOTTLE, SPRAY | SPRAY | 118.3 | 7 | |
| 69574-005-05 | NOVUMAPR | 1 in 1 BOX | SPRAY | 1 | 7 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| MENTHOL | ACTIVE INGREDIENT | L7T10EIP3A | NOVUM APR (MENTHOL) SPRAY [NOVUM SOLUTIONS INC] | 3 | |
| MENTHOL | ACTIVE MOIETY | L7T10EIP3A | NOVUM APR (MENTHOL) SPRAY [NOVUM SOLUTIONS INC] | 3 | |
| EUCALYPTUS OIL | INACTIVE INGREDIENT | 2R04ONI662 | NOVUM APR (MENTHOL) SPRAY [NOVUM SOLUTIONS INC] | 3 | |
| ISOPROPYL ALCOHOL | INACTIVE INGREDIENT | ND2M416302 | NOVUM APR (MENTHOL) SPRAY [NOVUM SOLUTIONS INC] | 3 | |
| METHYL SALICYLATE | INACTIVE INGREDIENT | LAV5U5022Y | NOVUM APR (MENTHOL) SPRAY [NOVUM SOLUTIONS INC] | 3 | |
| SPEARMINT OIL | INACTIVE INGREDIENT | C3M81465G5 | NOVUM APR (MENTHOL) SPRAY [NOVUM SOLUTIONS INC] | 3 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | NOVUM APR (MENTHOL) SPRAY [NOVUM SOLUTIONS INC] | 3 |
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 |
|---|---|---|---|---|---|---|
| Nighttime 4X Medicated Cream | BENZOCAINE | Rite Aid | 21645ed1-2dc0-223a-e063-6394a90ab021 | 2025-11-21 | Warnings | M017 |
| 4x Medicated Gum Cream | BENZOCAINE | Albertsons | b81a308c-9c30-0e3d-e053-2a95a90a15d2 | 2025-11-21 | Warnings | M017 |
| MENTHOL, CAMPHOR | MENTHOL, CAMPHOR | SUNSET NOVELTIES, INC | b0edd9d9-951f-d3dd-e053-2995a90a8d5a | 2025-11-21 | Warnings | M017 |
| Up up | LIDOCAINE PAIN RELIEF MAXIMUM STRENGTH PATCHES | Target Corporation | 44121d40-86e1-0df6-e063-6294a90aedaf | 2025-11-20 | Warnings | M017 |
| Up up | PAIN RELIEF ADVANCED HYDROGEL PATCHES | Target Corporation | 44128b70-3172-ee37-e063-6294a90a705f | 2025-11-20 | Warnings | M017 |
| MENTHOL, CAMPHOR | MENTHOL, CAMPHOR | SUNSET NOVELTIES, INC | f03090fa-f7e6-f53a-e053-2a95a90aa819 | 2025-11-20 | Warnings | M017 |
| HEATING PAIN RELIEF | METHYL SALICYLATE, MENTHOL | SUNSET NOVELTIES, INC | ff073e47-3107-e17e-e053-6294a90a58fa | 2025-11-20 | Warnings | M017 |
| MENTHOL, CAMPHOR | MENTHOL, CAMPHOR | SUNSET NOVELTIES, INC | fc8a8f20-97ab-481e-e053-6394a90a3525 | 2025-11-20 | Warnings | M017 |
| MENTHOL | MENTHOL | SUNSET PAIN RELIEF ROLL-ON 3OZ | 934d4638-b47b-187d-e053-2995a90ae69d | 2025-11-20 | Warnings | M017 |
| FOOT PAIN RELIEF ROLL-ON | LIDOCAINE, MENTHOL | Guangzhou Zhupuyou E-commerce Co., Ltd | 43edcea0-ab04-f368-e063-6294a90a817a | 2025-11-19 | Warnings | M017 |
| Absolut Skin Corticosoothe Anti-Itch | HYDROCORTISONE | Absolut Skin Incorporated | deb52218-9176-4aaa-a22f-b66dada6690f | 2025-11-19 | Warnings | M017 |
| Maximum Strength 4% Lidocaine Patch Good Neighbor Pharmacy | LIDOCAINE | InterMed Laboratories Private Limited | 43f3d189-f6b7-02ed-e063-6394a90afd73 | 2025-11-19 | Warnings | M017 |
| Maximum Strength 4% Lidocaine Patch HealthA2Z | LIDOCAINE | InterMed Laboratories Private Limited | 43f3e288-e828-8130-e063-6394a90a6d44 | 2025-11-19 | Warnings | M017 |
| Maximum Strength 4% Lidocaine Patch Leader | LIDOCAINE | InterMed Laboratories Private Limited | 42f06914-c8b8-ea9c-e063-6294a90a79e6 | 2025-11-19 | Warnings | M017 |
| CVS Anti-Itch | CAMPHOR, MENTHOL | CVS | 87715662-c788-9a8d-e053-2a95a90acb53 | 2025-11-19 | Warnings | M017 |
| Walgreen Anti Itch | CAMPHOR, MENTHOL | Walgreens | b4f47a8d-d4a6-9233-e053-2a95a90afd90 | 2025-11-19 | Warnings | M017 |
| Leader Anti-Itch | CAMPHOR, MENTHOL | LEADER/Cardinal Helath 110, Inc. | 9ca985c6-5017-0558-e053-2995a90a8202 | 2025-11-19 | Warnings | M017 |
| CVS Anti-Itch | PRAMOXINE HCL | CVS | 87fc476a-5b12-7383-e053-2995a90a530b | 2025-11-19 | Warnings | M017 |
| Walgreen Anti-Itch | PRAMOXINE HCL | Walgreens | b5f9d1c5-891e-4377-e053-2995a90aa281 | 2025-11-19 | Warnings | M017 |
| MENTHOL, CAMPHOR | MENTHOL, CAMPHOR | SUNSET PAIN RELIEF | 89f5f688-856f-f2df-e053-2995a90a73cf | 2025-11-19 | Warnings | M017 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1314935 | menthol 0.5 % Topical Spray | PSN | 1b869a1f-5787-4d03-a546-43a8217b2b2c | 7 |
| 1314935 | menthol 5 MG/ML Topical Spray | SCD | 1b869a1f-5787-4d03-a546-43a8217b2b2c | 7 |
| 1314935 | menthol 0.5 % Topical Spray | SY | 1b869a1f-5787-4d03-a546-43a8217b2b2c | 7 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 69574-005-04 | 69574000504 | 118.3 mL in 1 BOTTLE, SPRAY | 118.3 ml | Historical | ||||
| 69574-005-05 | 69574000505 | 1 BOTTLE, SPRAY in 1 BOX (69574-005-05) / 118.3 mL in 1 BOTTLE, SPRAY (69574-005-04) | 2015-05-19 | 0000-00-00 | No | No | Current |