Home NDC 66902-116 Fast Freeze Pain Relieving
Product NDC 66902-116
11-digit product format 669020116
Labeler code 66902
Product ID 66902-116_3ca5d610-63fa-a6f3-e063-6394a90a85b1
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL, UNSPECIFIED FORM
Dosage form GEL
Route TOPICAL
Labeler NATURAL ESSENTIALS, INC.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-03-31
Substance MENTHOL, UNSPECIFIED FORM
Active strength 33 mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Fast Freeze Pain Relieving
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL, UNSPECIFIED FORM 33 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 66902-116-03 Fast Freeze Pain Relieving 89 mL in 1 CONTAINER GEL 89 4 66902-116-04 Fast Freeze Pain Relieving 120 mL in 1 TUBE GEL 120 4 66902-116-36 Fast Freeze Pain Relieving 89 mL in 1 BOTTLE GEL 89 4 66902-116-36 Fast Freeze Pain Relieving 12 in 1 CASE GEL 12 4 66902-116-48 Fast Freeze Pain Relieving 120 mL in 1 TUBE GEL 120 4 66902-116-48 Fast Freeze Pain Relieving 12 in 1 CASE GEL 12 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 66902-116 FAST FREEZE PAIN RELIEVING (MENTHOL, UNSPECIFIED FORM) GEL [NATURAL ESSENTIALS, INC.] 3 Current NDC, Legacy NDC, 6 package rows 20241006_15a26af1-ca5a-40fc-a411-6c0e8ae18fbb.zip
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 8 of 156 · 3,115 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 66902-116-03 66902011603 89 mL in 1 CONTAINER (66902-116-03) 89 ml 2021-03-31 0000-00-00 No No Current 66902-116-04 66902011604 120 mL in 1 TUBE (66902-116-04) 120 ml 2021-10-06 0000-00-00 No No Current 66902-116-36 66902011636 12 BOTTLE in 1 CASE (66902-116-36) / 89 mL in 1 BOTTLE 12 bottle 2025-08-01 No No Current 66902-116-48 66902011648 12 TUBE in 1 CASE (66902-116-48) / 120 mL in 1 TUBE 12 tube 2025-08-01 No No Current