Feminine Comfort NDC 55714-2438

NDC codes

FDA NDC Directory

Product NDC (as listed)55714-2438Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55714-2438Add 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
55714-2438-1	55714243801	30 mL in 1 BOTTLE, GLASS (55714-2438-1)Marketed from Jan 31, 2019

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): Feminine Comfort
Generic name (nonproprietary): agaricus musc., arsenicum alb., aur. met., berber. aqui., caladium seguinum, candida albicans, cantharis, conium, graphites, helonias dioica, hydrastis, kali carb., kreosotum, lycopodium, merc. viv., murex purpurea, nat. mur., nitricum ac., pulsatilla, rhus toxicodendron, sepia, sulphur, tarentula hispana, thuja occ., zinc. met., apis mel., hamamelis
Active ingredients: Amanita muscaria fruiting body — 15 [hp_X]/mLArsenic trioxide — 15 [hp_X]/mLGold — 15 [hp_X]/mLBerberis aquifolium root bark — 15 [hp_X]/mLDieffenbachia seguine — 15 [hp_X]/mLCandida albicans — 15 [hp_X]/mLLytta vesicatoria — 15 [hp_X]/mLConium maculatum flowering top — 15 [hp_X]/mLGraphite — 15 [hp_X]/mLChamaelirium luteum root — 15 [hp_X]/mLGoldenseal — 15 [hp_X]/mLPotassium carbonate — 15 [hp_X]/mLWood creosote — 15 [hp_X]/mLLycopodium clavatum spore — 15 [hp_X]/mLMercury — 15 [hp_X]/mLHexaplex trunculus hypobranchial gland juice — 15 [hp_X]/mLSodium chloride — 15 [hp_X]/mLNitric acid — 15 [hp_X]/mLAnemone pulsatilla — 15 [hp_X]/mLToxicodendron pubescens leaf — 15 [hp_X]/mLSepia officinalis juice — 15 [hp_X]/mLSulfur — 15 [hp_X]/mLLycosa tarantula — 15 [hp_X]/mLThuja occidentalis leafy twig — 15 [hp_X]/mLZinc — 15 [hp_X]/mLApis mellifera — 6 [hp_X]/mLHamamelis virginiana root bark/stem bark — 6 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Newton Laboratories, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 31, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 55714-2438_b4f501d4-ae0b-a190-e053-2a95a90aae3aSPL ID b4f501d4-ae0b-a190-e053-2a95a90aae3aSPL set ID 9ab4520d-1dd3-7b9f-e053-2a95a90a274fUNII DIF093I037, S7V92P67HO, 79Y1949PYO, VZJ9F3C3SB, 01800C6E6B, 4D7G21HDBC, 3Q034RO3BT, Q28R5GF371, 4QQN74LH4O, DQV54Y5H3U, ZW3Z11D0JV, BQN1B9B9HA, 3JYG22FD73, C88X29Y479, FXS1BY2PGL, IQV54TN60Y, 451W47IQ8X, 411VRN1TV4, I76KB35JEV, 6IO182RP7A, QDL83WN8C2, 70FD1KFU70, 86M454L2TT, 1NT28V9397, J41CSQ7QDS, 7S82P3R43Z, T7S323PKJS
Pharmacologic class: Non-Standardized Fungal Allergenic Extract; Standardized Chemical Allergen; Standardized Insect Venom 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

N455714243801 followed by a unit qualifier and the quantity

Package 55714-2438-01. 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 Nov 25, 2020.

Indications (excerpt from the label)

INDICATIONS & USAGE SECTION Formulated for symptoms associated with vaginal discomfort such as itching, burning, dryness, irritation, soreness and discharge.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)