Pain Relieving Cold Therapy

Product NDC
68678-051
11-digit product format
686780051
Labeler code
68678
Product ID
68678-051_3dd5fbd3-2a69-9d53-e063-6294a90a40bb
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
GEL
Route
TOPICAL
Labeler
AHC VENTURES CORP DBA CRYODERM
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2016-01-01
Substance
MENTHOL
Active strength
10 g/100L
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Pain Relieving Cold Therapy
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL10 g/100L

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68678-051-382025-09-02C16284748780-11030e365-6ad6-111a-e063-dadaa90a10e2Pain Relieving Cold Therapy
68678-051-382024-01-30C16284748780-11030e365-6ad6-111a-e063-dadaa90a10e2Pain Relieving Cold Therapy

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68678-051-38Pain Relieving Cold Therapy4.2 L in 1 BOTTLE, DISPENSINGGEL4.22

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68678-051PAIN RELIEVING COLD THERAPY (MENTHOL) GEL [AHC VENTURES CORP DBA CRYODERM]1Current NDC, Legacy NDC, 1 package rows20220504_de210c3a-c24e-cefd-e053-2a95a90a93ff.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68678-051-38686780051384.2 L in 1 BOTTLE, DISPENSING (68678-051-38) 4.2 l2016-01-010000-00-00NoNoCurrent