Home NDC 24330-210 SunBurnt Advanced After-Sun
Product NDC 24330-210
11-digit product format 243300210
Labeler code 24330
Product ID 24330-210_3d715022-70be-44aa-bfa3-f37823e35421
Type HUMAN OTC DRUG
Nonproprietary name Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria
Dosage form GEL
Route TOPICAL
Labeler Welmedix LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2007-01-01
Substance CALENDULA OFFICINALIS FLOWER; ECHINACEA ANGUSTIFOLIA; LYTTA VESICATORIA
Active strength 1; 1; 3 [hp_Q]/.1g; [hp_Q]/.1g; [hp_X]/.1g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 24 matching rows.
View current auxiliary records. · View the auxiliary file history.
Additional Listing Data#
Finished product Yes
Brand name base SunBurnt Advanced After-Sun
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALENDULA OFFICINALIS FLOWER 1 [hp_Q]/.1g ECHINACEA ANGUSTIFOLIA 1 [hp_Q]/.1g LYTTA VESICATORIA 3 [hp_X]/.1g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination P0M7O4Y7YD Internal UNII lookup VB06AV5US8 Internal UNII lookup 3Q034RO3BT Internal UNII 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 24330-210-01 SunBurnt Advanced After-Sun 7.1 g in 1 TUBE GEL 7.1 4 24330-210-01 SunBurnt Advanced After-Sun 1 in 1 POUCH GEL 1 4 24330-210-03 SunBurnt Advanced After-Sun 1 in 1 CARTON GEL 1 4 24330-210-03 SunBurnt Advanced After-Sun 71 g in 1 TUBE GEL 71 4 24330-210-06 SunBurnt Advanced After-Sun 170 g in 1 TUBE GEL 170 4 24330-210-06 SunBurnt Advanced After-Sun 1 in 1 CARTON GEL 1 4 24330-210-21 SunBurnt Advanced After-Sun 1 in 1 CARTON GEL 1 4 24330-210-21 SunBurnt Advanced After-Sun 21.3 g in 1 TUBE GEL 21.3 4
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded CALENDULA OFFICINALIS FLOWER ACTIVE INGREDIENT P0M7O4Y7YD SUNBURNT (CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA) TINCTURE [WELMEDIX LLC] 3 ECHINACEA ANGUSTIFOLIA ACTIVE INGREDIENT VB06AV5US8 SUNBURNT (CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA) TINCTURE [WELMEDIX LLC] 3 LYTTA VESICATORIA ACTIVE INGREDIENT 3Q034RO3BT SUNBURNT (CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA) TINCTURE [WELMEDIX LLC] 3 CALENDULA OFFICINALIS FLOWER ACTIVE MOIETY P0M7O4Y7YD SUNBURNT (CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA) TINCTURE [WELMEDIX LLC] 3 ECHINACEA ANGUSTIFOLIA ACTIVE MOIETY VB06AV5US8 SUNBURNT (CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA) TINCTURE [WELMEDIX LLC] 3 LYTTA VESICATORIA ACTIVE MOIETY 3Q034RO3BT SUNBURNT (CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA) TINCTURE [WELMEDIX LLC] 3 ALOE VERA LEAF INACTIVE INGREDIENT ZY81Z83H0X SUNBURNT (CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA) TINCTURE [WELMEDIX LLC] 3 CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) INACTIVE INGREDIENT 71DD5V995L SUNBURNT (CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA) TINCTURE [WELMEDIX LLC] 3 HYALURONATE SODIUM INACTIVE INGREDIENT YSE9PPT4TH SUNBURNT (CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA) TINCTURE [WELMEDIX LLC] 3 PANTHENOL INACTIVE INGREDIENT WV9CM0O67Z SUNBURNT (CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA) TINCTURE [WELMEDIX LLC] 3 PHENOXYETHANOL INACTIVE INGREDIENT HIE492ZZ3T SUNBURNT (CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA) TINCTURE [WELMEDIX LLC] 3 SODIUM HYDROXIDE INACTIVE INGREDIENT 55X04QC32I SUNBURNT (CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA) TINCTURE [WELMEDIX LLC] 3 WATER INACTIVE INGREDIENT 059QF0KO0R SUNBURNT (CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA) TINCTURE [WELMEDIX LLC] 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 24330-210 SUNBURNT ADVANCED AFTER-SUN (CALENDULA OFFICINALIS, ECHINACEA ANGUSTIFOLIA, CANTHARIS VESICATORIA) GEL [WELMEDIX LLC] 4 Current NDC, Legacy NDC, 8 package rows 20180404_dcb2fd62-df8e-4a26-b7ed-274caefeeb76.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 1 of 1 · 1 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 24330-210-01 24330021001 7.1 g in 1 TUBE 7.1 g Historical 24330-210-03 24330021003 1 TUBE in 1 CARTON (24330-210-03) / 71 g in 1 TUBE 1 tube 2016-09-01 0000-00-00 No No Current 24330-210-06 24330021006 1 TUBE in 1 CARTON (24330-210-06) / 170 g in 1 TUBE 1 tube 2016-09-01 0000-00-00 No No Current 24330-210-21 24330021021 1 in 1 CARTON Historical