NDC codes

FDA NDC Directory
Product NDC (as listed)24330-210Labeler and product segments. Claims need a package NDC.
Product NDC at billing width24330-0210Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
24330-210-0324330021003243300210031 TUBE in 1 CARTON (24330-210-03) / 71 g in 1 TUBEMarketed from Sep 1, 2016
24330-210-0624330021006243300210061 TUBE in 1 CARTON (24330-210-06) / 170 g in 1 TUBEMarketed from Sep 1, 2016

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
SunBurnt Advanced After-Sun
Generic name (nonproprietary)
calendula officinalis, echinacea angustifolia, cantharis vesicatoria
Active ingredients
Calendula officinalis flower — 1 [hp_Q]/.1gEchinacea angustifolia — 1 [hp_Q]/.1gLytta vesicatoria — 3 [hp_X]/.1g
Dosage form
Gel
Route
Topical
Labeler
Welmedix LLCNDC labeler code 24330
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 24330-210_3d715022-70be-44aa-bfa3-f37823e35421SPL ID 3d715022-70be-44aa-bfa3-f37823e35421SPL set ID dcb2fd62-df8e-4a26-b7ed-274caefeeb76UNII P0M7O4Y7YD, VB06AV5US8, 3Q034RO3BT

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N424330021003 followed by a unit qualifier and the quantity

Package 24330-0210-03. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Uses Temporarily relieves symptoms of mild and moderate sunburn such as: overheated skin redness rawness itching dryness Product Uses are based on the Homeopathic Materia Medica. These Uses have not been evaluated by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 24330-210

What is NDC 24330-210?
24330-210 is the product NDC for SunBurnt Advanced After-Sun, Calendula officinalis flower 1 [hp_Q]/.1g + 2 more ingredients gel, listed with the FDA by Welmedix LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
SunBurnt Advanced After-Sun (Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria).
What is the active ingredient?
Calendula officinalis flower, Echinacea angustifolia, Lytta vesicatoria.
Who is the labeler?
Welmedix LLC, NDC labeler code 24330. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for SunBurnt Advanced After-Sun?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

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