Home NDC 52000-113 Universal Vaporizing Chest Rub
Product NDC 52000-113
11-digit product format 520000113
Labeler code 52000
Product ID 52000-113_b404496d-fd70-4d79-b4fb-1cb0e73fe292
Type HUMAN OTC DRUG
Nonproprietary name Menthol and Camphor and Eucalyptus
Dosage form OINTMENT
Route TOPICAL
Labeler Universal Distribution Center LLC
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-06-16
Substance CAMPHOR (SYNTHETIC); MENTHOL, UNSPECIFIED FORM; EUCALYPTUS OIL
Active strength 4.7; 1.25; 1 g/100g; g/100g; g/100g
NDC exclude flag No
Listing certified through 2027-12-31
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 Universal Vaporizing Chest Rub
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (SYNTHETIC) 4.7 g/100g MENTHOL, UNSPECIFIED FORM 1.25 g/100g EUCALYPTUS OIL 1 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5TJD82A1ET Internal UNII lookup L7T10EIP3A Internal UNII lookup 2R04ONI662 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2374740 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 52000-113-01 Universal Vaporizing Chest Rub 113 g in 1 BOTTLE, PLASTIC OINTMENT 113 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52000-113 UNIVERSAL VAPORIZING CHEST RUB (MENTHOL AND CAMPHOR AND EUCALYPTUS) OINTMENT [UNIVERSAL DISTRIBUTION CENTER LLC] 2 Current NDC, Legacy NDC, 1 package rows 20231121_b1d25572-da21-408d-aab3-3a0741dfff12.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 73 of 178 · 3,551 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 52000-113-01 52000011301 113 g in 1 BOTTLE, PLASTIC (52000-113-01) 113 g 2020-06-16 0000-00-00 No No Current