NDC 61577-3610
DEEP REMEDY
Menthol Camphor
DEEP REMEDY is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Sombra Cosmetics Inc.. The primary component is Menthol; Camphor (synthetic).
| Product ID | 61577-3610_1fb514f2-a819-4350-94c5-d1606b4bbe5f |
| NDC | 61577-3610 |
| Product Type | Human Otc Drug |
| Proprietary Name | DEEP REMEDY |
| Generic Name | Menthol Camphor |
| Dosage Form | Gel |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2013-01-01 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part348 |
| Labeler Name | SOMBRA COSMETICS INC. |
| Substance Name | MENTHOL; CAMPHOR (SYNTHETIC) |
| Active Ingredient Strength | 0 g/g; g/g |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
Packaging
NDC 61577-3610-1
14.2 g in 1 JAR (61577-3610-1)
| Marketing Start Date | 2021-12-23 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 61577-3610-2 [61577361002]
DEEP REMEDY GEL
| Marketing Category | OTC monograph not final |
| Application Number | part348 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2013-01-01 |
| Inactivation Date | 2020-01-31 |
NDC 61577-3610-5 [61577361005]
DEEP REMEDY GEL
| Marketing Category | OTC monograph not final |
| Application Number | part348 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2013-01-01 |
| Inactivation Date | 2020-01-31 |
NDC 61577-3610-4 [61577361004]
DEEP REMEDY GEL
| Marketing Category | OTC monograph not final |
| Application Number | part348 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2013-01-01 |
| Inactivation Date | 2020-01-31 |
NDC 61577-3610-8 [61577361008]
DEEP REMEDY GEL
| Marketing Category | OTC monograph not final |
| Application Number | part348 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2013-01-01 |
| Inactivation Date | 2020-01-31 |
NDC 61577-3610-1 [61577361001]
DEEP REMEDY GEL
| Marketing Category | OTC monograph not final |
| Application Number | part348 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2013-01-01 |
| Inactivation Date | 2020-01-31 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| MENTHOL | .03 g/g |
OpenFDA Data
| SPL SET ID: | dcfd0511-39d9-4221-b111-947f0785e043 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
NDC Crossover Matching brand name "DEEP REMEDY" or generic name "Menthol Camphor"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 61577-3610 | DEEP REMEDY | MENTHOL CAMPHOR |
| 59321-011 | Gold Edition Ultra Zheng Gu Shui | Menthol Camphor |
| 61577-3501 | GREEN BAMBOO | MENTHOL CAMPHOR |
| 61577-4080 | HealQu Warm Therapy Gel | MENTHOL CAMPHOR |
| 61821-100 | Hua Tuo | Menthol Camphor |
| 73412-001 | Hua Tuo | Menthol Camphor |
| 20276-210 | Lucky Blue Ice | Menthol Camphor |
| 47046-167 | Lucky Blue Ice | Menthol Camphor |
| 61577-2301 | MUSCLE EASE | MENTHOL CAMPHOR |
| 72380-521 | OPITOX TOPICAL | MENTHOL CAMPHOR |
| 61577-7365 | PAIN NO MORE THERAPY | MENTHOL CAMPHOR |
| 61577-5310 | SNAP CRACK | MENTHOL CAMPHOR |
| 61577-7050 | Sombra CBD Warm Therapy | Menthol Camphor |
| 61577-7010 | Sombra Plus CBD 1000mg Warm Theapy | Menthol Camphor |
| 61577-7120 | Sombra Plus CBD 2000mg Warm Theapy | Menthol Camphor |
| 61577-3216 | SOMBRA WARM THERAPY | MENTHOL CAMPHOR |
| 61577-4020 | SOMBRA WARM THERAPY | MENTHOL CAMPHOR |
| 61577-2280 | SORE NO MORE | MENTHOL CAMPHOR |
| 61577-7011 | Sore No More Warm Therapry Plus CBD 1000mg | Menthol Camphor |
| 61577-7012 | Sore No More Warm Therapry Plus CBD 2000mg | Menthol Camphor |
| 61577-7055 | Sore No More Warm Therapy Plus CBD 500mg Natural Pain Relieving Gel | Menthol Camphor |
| 61577-1400 | Tonys Warm Therapy | Menthol Camphor |
Trademark Results [DEEP REMEDY]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 DEEP REMEDY 85731422 4433702 Live/Registered |
Deep Remedy Inc. 2012-09-18 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.