Acne

Product NDC
69607-0001
11-digit product format
696070001
Labeler code
69607
Product ID
69607-0001_040e8c01-1cd6-4241-8e03-59ef13ef8e04
Type
HUMAN OTC DRUG
Nonproprietary name
Anthracinum, Antimonium crudum, Hydrocotyle asiatica, Juglans regia, Kali bromatum, Ledum palustre, Natrum sulphuratum, Pyrogenium, Radium bromatum, Sanguinaria canadensis, Sulphur iodatum, Thuja occidentalis, Uritica urens
Dosage form
SPRAY
Route
ORAL
Labeler
Biovea
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-07-07
Marketing end
2022-03-31
Substance
ANTIMONY TRISULFIDE; BACILLUS ANTHRACIS IMMUNOSERUM RABBIT; CENTELLA ASIATICA; JUGLANS REGIA FRUIT RIND, IMMATURE; JUGLANS REGIA LEAF; LEDUM PALUSTRE TWIG; POTASSIUM BROMIDE; RADIUM BROMIDE; RANCID BEEF; SANGUINARIA CANADENSIS ROOT; SODIUM SULFIDE NONAHYDRATE; SULFUR IODIDE; THUJA OCCIDENTALIS LEAFY TWIG; URTICA URENS
Active strength
30 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL
Pharmacologic classes
Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69607-0001-12022-03-09C16284748780-19d75b9cf-ef21-f424-e053-dadaa90a57ce1946dbcf-4b6d-44f8-ad9e-466226886d26
69607-0001-12020-01-31C16284748780-19d75b9cf-ef21-f424-e053-dadaa90a57ce1946dbcf-4b6d-44f8-ad9e-466226886d26

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69607-0001-16960700010130 mL in 1 BOTTLE, SPRAY (69607-0001-1) 30 ml2015-07-072022-03-31NoNoCurrent