NDC 24357-701-01 - Anecream
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 24357-701
- Requested NDC
- 24357-701-01
- Package NDCs from labels
- 24357-701-30, 24357-701-15, 24357-701-05, 24357-701-07, 24357-701-06, 24357-701-01, 24357-701-50
- Manufacturer
- Focus Health Group
- Effective date
- 2025-01-15
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Anecream - Focus Health Group | Focus Health Group | 2025-01-15 | HUMAN OTC DRUG LABEL |
| Anecream 4% | REMEDYREPACK INC. | 2017-12-20 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 24357-701-01 | Anecream | 2.5 g in 1 PACKET | CREAM | 2.5 | 13 | |
| 24357-701-05 | Anecream | 5 g in 1 TUBE | CREAM | 5 | 13 | |
| 24357-701-06 | Anecream | 5 in 1 CARTON | CREAM | 5 | 13 | |
| 24357-701-07 | Anecream | 5 in 1 CARTON | CREAM | 5 | 13 | |
| 24357-701-15 | Anecream | 15 g in 1 TUBE | CREAM | 15 | 13 | |
| 24357-701-15 | Anecream | 1 in 1 CARTON | CREAM | 1 | 13 | |
| 24357-701-30 | Anecream | 1 in 1 CARTON | CREAM | 1 | 13 | |
| 24357-701-30 | Anecream | 30 g in 1 TUBE | CREAM | 30 | 13 | |
| 24357-701-50 | Anecream | 50 in 1 CARTON | CREAM | 50 | 13 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 24357-701-07 | EA - Each | 24357-701 | 6bf9f8b6-794a-4ca7-901d-4ffcb2ceec98 | 1 | 2012-07-24 |
| 24357-701-15 | GM - Gram | 24357-701 | b90de22f-c3c4-42b8-9da2-ba9fec674c4a | 1 | 2012-07-24 |
| 24357-701-30 | GM - Gram | 24357-701 | 9ce9ab87-2ce7-4039-857d-b97202adf4cd | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
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 |
|---|---|---|---|---|---|---|
| Aspercreme Lidocaine Foot (Diabetic) | LIDOCAINE HYDROCHLORIDE | Chattem, Inc. | 2c33d15e-5032-46d9-bd98-5abc7df3bbe5 | 2026-01-13 | Warnings | M017 |
| Aspercreme with Lidocaine Essential Oils Rosemary Mint | LIDOCAINE | Chattem, Inc. | 9c81d5eb-fa9b-47fb-8924-6ebf6a5c6bab | 2026-01-13 | Warnings | M017 98PI200987 |
| Capzasin HP Arthritis Pain Relief | CAPSAICIN | Chattem, Inc. | 345c9159-0efe-436b-9068-3b717678936b | 2026-01-13 | Warnings | M017 |
| Capzasin Quick Relief | CAPSAICIN AND MENTHOL | Chattem, Inc. | d6c313a3-8dc6-4231-95b6-ac9399e1c1be | 2026-01-13 | Warnings | M017 |
| Aspercreme Pain Relieving | TROLAMINE SALICYLATE | Chattem, Inc. | 97dd587b-ecc3-4b4b-a116-6355d3c6ea6d | 2026-01-13 | Warnings | M017 |
| Lidocaine 5% Patch | LIDOCAINE 5% | Medcore LLC | 1afe428f-e223-4ef8-a6ba-968f4cfbf476 | 2026-01-12 | Warnings, Adverse reactions | 98PI200987 |
| Dr Wellskin Numbing Cream | 4% LIDOCAINE | Shengnan (Guangzhou) Cosmetics Co., LTD | 482f25cc-dee3-c3b6-e063-6294a90a8674 | 2026-01-12 | Warnings | M017 98PI200987 |
| BLT 2 | LIDOCAINE HCL | CENTURA PHARMACEUTICALS INC | 41dc85ec-d79b-0a32-e054-00144ff8d46c | 2026-01-12 | Warnings | M017 |
| Mineral Ice Pain Relieving | MENTHOL | Crown Laboratories | 7b30076a-0af6-2f74-e053-2a91aa0ae08d | 2026-01-12 | Warnings | M017 |
| 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 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.