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 table
LabelManufacturerEffective dateType
Anecream - Focus Health GroupFocus Health Group2025-01-15HUMAN OTC DRUG LABEL
Anecream 4%REMEDYREPACK INC.2017-12-20HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
24357-701-01Anecream2.5 g in 1 PACKETCREAM2.513
24357-701-05Anecream5 g in 1 TUBECREAM513
24357-701-06Anecream5 in 1 CARTONCREAM513
24357-701-07Anecream5 in 1 CARTONCREAM513
24357-701-15Anecream15 g in 1 TUBECREAM1513
24357-701-15Anecream1 in 1 CARTONCREAM113
24357-701-30Anecream1 in 1 CARTONCREAM113
24357-701-30Anecream30 g in 1 TUBECREAM3013
24357-701-50Anecream50 in 1 CARTONCREAM5013

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
24357-701ANECREAM (LIDOCAINE 4%) CREAM [FOCUS HEALTH GROUP]13Current NDC, Legacy NDC, 9 package rows20250126_2d7706e2-7363-4047-96cb-85b718277e8c.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
24357-701-07EA - Each24357-7016bf9f8b6-794a-4ca7-901d-4ffcb2ceec9812012-07-24
24357-701-15GM - Gram24357-701b90de22f-c3c4-42b8-9da2-ba9fec674c4a12012-07-24
24357-701-30GM - Gram24357-7019ce9ab87-2ce7-4039-857d-b97202adf4cd12012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LIDOCAINEACTIVE INGREDIENT98PI200987ANECREAM (LIDOCAINE 4%) CREAM [FOCUS HEALTH GROUP]1
LIDOCAINEACTIVE MOIETY98PI200987ANECREAM (LIDOCAINE 4%) CREAM [FOCUS HEALTH GROUP]1
.ALPHA.-TOCOPHEROL ACETATE, DL-INACTIVE INGREDIENTWR1WPI7EW8ANECREAM (LIDOCAINE 4%) CREAM [FOCUS HEALTH GROUP]1
BENZYL ALCOHOLINACTIVE INGREDIENTLKG8494WBHANECREAM (LIDOCAINE 4%) CREAM [FOCUS HEALTH GROUP]1
CARBOMER HOMOPOLYMER TYPE CINACTIVE INGREDIENT4Q93RCW27EANECREAM (LIDOCAINE 4%) CREAM [FOCUS HEALTH GROUP]1
CHOLESTEROLINACTIVE INGREDIENT97C5T2UQ7JANECREAM (LIDOCAINE 4%) CREAM [FOCUS HEALTH GROUP]1
LECITHIN, SOYBEANINACTIVE INGREDIENT1DI56QDM62ANECREAM (LIDOCAINE 4%) CREAM [FOCUS HEALTH GROUP]1
POLYSORBATE 80INACTIVE INGREDIENT6OZP39ZG8HANECREAM (LIDOCAINE 4%) CREAM [FOCUS HEALTH GROUP]1
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3ANECREAM (LIDOCAINE 4%) CREAM [FOCUS HEALTH GROUP]1
TROLAMINEINACTIVE INGREDIENT9O3K93S3TKANECREAM (LIDOCAINE 4%) CREAM [FOCUS HEALTH GROUP]1
WATERINACTIVE INGREDIENT059QF0KO0RANECREAM (LIDOCAINE 4%) CREAM [FOCUS HEALTH GROUP]1

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.

Matched openFDA labels page 64 of 194 · 3,864 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Ted and Gregs Pain Rub with Resveratrol Topical AnalgesicMETHYL SALICYLATETed and Greg's Inc.c699438d-595d-4711-801b-51e960aa36682025-12-29WarningsExact identifier
application number: M017
Frankincense and Myrrh Arthritis Pain Combo PackMENTHOLWISE CONSUMER PRODUCTS CO.47199677-e04c-768b-e063-6294a90a35242025-12-29WarningsExact identifier
application number: M017
Witch HazelWITCH HAZELCVS HEALTHb8b79e8d-9c84-1700-e053-2995a90af5bd2025-12-29WarningsExact identifier
application number: M017
WALGREENS BURNLIDOCAINE HYDROCHLORIDEWALGREENSb61e6d73-4f41-ef50-e053-2a95a90a0fc62025-12-29WarningsExact identifier
application number: M017
CVS cold and HotMENTHOL 16%CVSd1676df9-530f-1664-e053-2995a90a5b642025-12-29WarningsExact identifier
application number: M017
HydrocortisoneHYDROCORTISONEAKRON PHARMA INCfa956b6a-1712-4f7a-9490-11866dcd17c82025-12-29WarningsExact identifier
application number: M017
Frankincense and Myrrh Nerve Combo PackMENTHOLWise Consumer Products471d815c-1c34-e0f8-e063-6294a90aca782025-12-29WarningsExact identifier
application number: M017
Pain ReleaseMENTHOLNatures Formulae Health Products Ltd.781d3c8d-7b70-e973-e053-2991aa0aaa782025-12-29WarningsExact identifier
application number: M017
Pain ReleaseMENTHOLNatures Formulae Health Products Ltd.781dfd66-f006-a2d7-e053-2991aa0a170c2025-12-29WarningsExact identifier
application number: M017
Pain ReleaseMENTHOLNatures Formulae Health Products Ltd.781d53cf-b3df-3e2b-e053-2a91aa0a7dcd2025-12-29WarningsExact identifier
application number: M017
Trauma LessMENTHOLNatures Formulae Health Products Ltd.781e94d5-1d34-7202-e053-2991aa0ae7682025-12-29WarningsExact identifier
application number: M017
Quality Choice Cold Therapy GelMENTHOLChain Drug Marketing Association, Inc.f9c659cd-e7fa-ac2d-e053-6294a90a25732025-12-29WarningsExact identifier
application number: M017
PAIN RELIEF PATCHESLIDOCAINEHarris Teeter5a0501e8-bc06-4e33-8db8-93b21a7151412025-12-29WarningsExact identifier
application number: M017
unii: 98PI200987
Hot and Cold Medicated PatchMENTHOLHarris Teeter9debd4ef-c21b-41ae-afd1-58f47c51c99c2025-12-29WarningsExact identifier
application number: M017
Maximum OTC Strength Feminine Anti-Itch CremeBENZOCAINE, RESORCINOLQuality Choice (CHAIN DRUG MARKETING ASSOCIATION)0e9a711c-ddf4-af63-e063-6294a90a0ebe2025-12-29WarningsExact identifier
application number: M017
Pain Relief PatchesCAMPHOR, MENTHOL, METHYL SALICYLATEHarris Teeter3f5b4eee-49c4-408c-9af2-e7924c26ac632025-12-29WarningsExact identifier
application number: M017
talc-free medicated bodyMENTHOLDavion, Inc27b9b4dc-4d4f-4e9d-b388-a7c6807a0e9b2025-12-29WarningsExact identifier
application number: M017
H-E-B Medicated Corn Starch Foot PowderMENTHOLDavion, Inca6675e00-bc6b-4466-a283-4cece5f919702025-12-29WarningsExact identifier
application number: M017
Maximum Strength Medicated Foot PowderMENTHOLDavion, Inc7b442d99-ac19-4f65-828d-954c5350ef5a2025-12-29WarningsExact identifier
application number: M017
OCUFRESHWATEROptics Laboratory Inc.b8e477a9-66b9-496b-92fb-3d4bbd7b36b52025-12-29WarningsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.