Home NDC 10210-0102 Carmex 10 count variety pack Lip Balm
Product NDC 10210-0102
11-digit product format 102100102
Labeler code 10210
Product ID 10210-0102_50afd74a-6bd9-3b73-e063-6394a90a3886
Type HUMAN OTC DRUG
Nonproprietary name OCTINOXATE, OXYBENZONE, CAMPHOR (SYNTHETIC), WHITE PETROLATUM
Dosage form KIT
Labeler Carma Laboratories, Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-01
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 Carmex 10 count variety pack Lip Balm
Listing expiration 2027-12-31 Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2475168 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 10210-0102-1 10210010201 1 KIT in 1 KIT (10210-0102-1) * 10 g in 1 TUBE (10210-0022-6) * 4.25 g in 1 CYLINDER (10210-0023-1) * 4.25 g in 1 CYLINDER (10210-0031-1) 1 kit 2026-08-01 No No Current