Pain Relieving Cold Therapy

Product NDC
68678-050
11-digit product format
686780050
Labeler code
68678
Product ID
68678-050_3dd631dc-3173-b10d-e063-6394a90a9da7
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
68678-050-322025-09-02C16284748780-11030e365-4f82-111a-e063-dadaa90a10e2Pain Relieving Cold Therapy
68678-050-322024-01-30C16284748780-11030e365-4f82-111a-e063-dadaa90a10e2Pain Relieving Cold Therapy

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68678-050-32Pain Relieving Cold Therapy1 L in 1 BOTTLE, DISPENSINGGEL12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68678-050PAIN RELIEVING COLD THERAPY (MENTHOL) GEL [AHC VENTURES CORP DBA CRYODERM]1Current NDC, Legacy NDC, 1 package rows20220504_de0c9a73-dbc0-599e-e053-2a95a90a7986.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68678-050-32686780050321 L in 1 BOTTLE, DISPENSING (68678-050-32) 1 l2016-01-010000-00-00NoNoCurrent