Herpes Simplex Plus

Product NDC

43742-1662

11-digit product format

437421662

Labeler code

43742

Product ID

43742-1662_a0aee502-5a9e-4610-af34-a1a105aaf330

Type

HUMAN OTC DRUG

Nonproprietary name

Allium Sativum, Calendula Officinalis, Sambucus Nigra, Clematis Erecta, Dulcamara, Sarsaparilla (Smilax Regelii), Graphites, Petroleum, Arsenicum Album, Croton Tiglium, Mercurius Sulphuratus Ruber, Natrum Muriaticum, Nitricum Acidum, Rhus Tox, Sepia, Thuja Occidentalis

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals,Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2020-06-29

Marketing end

2025-09-01

Substance

GARLIC; CALENDULA OFFICINALIS FLOWERING TOP; SAMBUCUS NIGRA FLOWERING TOP; CLEMATIS RECTA FLOWERING TOP; SOLANUM DULCAMARA TOP; SMILAX ORNATA ROOT; GRAPHITE; KEROSENE; ARSENIC TRIOXIDE; CROTON TIGLIUM SEED; MERCURIC SULFIDE; SODIUM CHLORIDE; NITRIC ACID; TOXICODENDRON PUBESCENS LEAF; SEPIA OFFICINALIS JUICE; THUJA OCCIDENTALIS LEAFY TWIG

Active strength

2 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record