CICATRISAN Cream NDC 62106-3152

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-3152Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-3152Add 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 NDC	11-digit (billing)	Package	Copy
62106-3152-0	62106315200	1 TUBE in 1 CARTON (62106-3152-0) / 40 g in 1 TUBEMarketed from May 7, 2015

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): CICATRISAN Cream
Generic name (nonproprietary): calendula officinalis, phytolacca decandra, bryonia dioica, balsamum peruvianum, dulcamara
Active ingredients: Balsam peru — 1 [hp_X]/40gBryonia dioica root — 1 [hp_X]/40gSolanum dulcamara top — 1 [hp_X]/40gCalendula officinalis flowering top — 1 [hp_X]/40gPhytolacca americana root — 1 [hp_X]/40g
Dosage form: Cream
Route: Topical
Labeler: Seroyal USA
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 7, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 62106-3152_c71eb176-d09b-45b3-e053-2a95a90a53dfSPL ID c71eb176-d09b-45b3-e053-2a95a90a53dfSPL set ID 156ec27b-d27e-1739-e054-00144ff88e88UNII 8P5F881OCY, 53UB5FH7CX, KPS1B1162N, 18E7415PXQ, 11E6VI8VEG
Pharmacologic class: Standardized Chemical Allergen

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

N462106315200 followed by a unit qualifier and the quantity

Package 62106-3152-00. 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 Jul 14, 2021.

Indications (excerpt from the label)

Uses For the temporary relief of symptoms associated with minor skin irritations. Directions Adults: Apply a small amount on the affected area two to three times daily, or as recommended by your healthcare practitioner. May cover affected area with sterile gauze after each application. Children: Use under the direction of your healthcare practitioner.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)