Hers Plus NDC 43742-1876

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1876Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1876Add 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
43742-1876-1	43742187601	30 mL in 1 BOTTLE, DROPPER (43742-1876-1)Marketed from Nov 30, 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): Hers Plus
Generic name (nonproprietary): calendula officinalis, sambucus nigra, allium sativum, clematis erecta, dulcamara, sarsaparilla (smilax regelii), graphites, petroleum, arsenicum album, croton tiglium, mercurius sulphuratus ruber, natrum muriaticum, nitricum acidum, rhus tox, sepia, thuja occidentalis
Active ingredients: Calendula officinalis flowering top — 2 [hp_X]/mLSambucus nigra flowering top — 3 [hp_X]/mLGarlic — 6 [hp_X]/mLClematis recta flowering top — 6 [hp_X]/mLSolanum dulcamara top — 6 [hp_X]/mLSmilax ornata root — 6 [hp_X]/mLGraphite — 8 [hp_X]/mLKerosene — 8 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLCroton tiglium seed — 12 [hp_X]/mLMercuric sulfide — 12 [hp_X]/mLSodium chloride — 12 [hp_X]/mLNitric acid — 12 [hp_X]/mLToxicodendron pubescens leaf — 12 [hp_X]/mLSepia officinalis juice — 12 [hp_X]/mLThuja occidentalis leafy twig — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals,Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 30, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 43742-1876_473bff35-5772-4fe3-a79f-318eeae9024bSPL ID 473bff35-5772-4fe3-a79f-318eeae9024bSPL set ID e4636b80-f6c8-459c-8d0e-ff7801358b10UNII 18E7415PXQ, CT03BSA18U, V1V998DC17, 396421SP9F, KPS1B1162N, 2H1576D5WG, 4QQN74LH4O, 1C89KKC04E, S7V92P67HO, 0HK2GZK66E, ZI0T668SF1, 451W47IQ8X, 411VRN1TV4, 6IO182RP7A, QDL83WN8C2, 1NT28V9397UPC 0810151883946
Pharmacologic class: Non-Standardized Food Allergenic Extract

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

NDC on a medical claim

N443742187601 followed by a unit qualifier and the quantity

Package 43742-1876-01. 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 Apr 9, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • painful eruptions of lips • painful eruptions on genitals • fever • vesicular eruptions on lips • fatigue • vesicular eruptions on genitals • tingling of lips • irritability • body aches • burning urination These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)