ReBoost NDC 62795-4005

NDC codes

FDA NDC Directory

Product NDC (as listed)62795-4005Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62795-4005Add 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
62795-4005-9	62795400509	1 BOTTLE, PUMP in 1 CARTON (62795-4005-9) / 20 mL in 1 BOTTLE, PUMPMarketed from Feb 4, 2020

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): ReBoost
Generic name (nonproprietary): silver nitrate,euphorbia resinifera resin, calcium sulfide, goldenseal, potassium dichromate,luffa operculata fruit, sodium carbonate, echinacea unspecified, cairina moschata heart/liver autolysate and pulsatilla vulgaris
Active ingredients: Silver nitrate — 10 [hp_X]/20mLEuphorbia resinifera resin — 4 [hp_X]/20mLCalcium sulfide — 10 [hp_X]/20mLGoldenseal — 5 [hp_X]/20mLPotassium dichromate — 6 [hp_X]/20mLLuffa operculata fruit — 2 [hp_X]/20mLSodium carbonate — 6 [hp_X]/20mLPulsatilla vulgaris — 2 [hp_X]/20mLCairina moschata heart/liver autolysate — 20 [hp_X]/20mLEchinacea, Unspecified — 3 [hp_X]/20mL
Dosage form: Spray
Route: Nasal
Labeler: MediNatura
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 4, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 62795-4005_dc9cb3f4-8286-48c3-bfa0-0ed53a3840b1SPL ID dc9cb3f4-8286-48c3-bfa0-0ed53a3840b1SPL set ID cb8a8d2a-d9d2-4a71-9279-c5641a9126c6UNII 95IT3W8JZE, 1TI1O9028K, 1MBW07J51Q, ZW3Z11D0JV, T4423S18FM, C4MO6809HU, 45P3261C7T, I76KB35JEV, RN2HC612GY, 4N9P6CC1DX

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. Nasal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N462795400509 followed by a unit qualifier and the quantity

Package 62795-4005-09. 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 19, 2022.

Indications (excerpt from the label)

Uses Uses: To temporarily relieve nasal congestion. To reduce cold and flu symptoms such as sinus headache & pressure.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)