A-19

Product NDC
58264-0311
11-digit product format
582640311
Labeler code
58264
Product ID
58264-0311_2b50cfc6-9de9-6371-e063-6294a90a7de4
Type
HUMAN OTC DRUG
Nonproprietary name
SOLENOPSIS INVICTA, PERIPLANETA AMERICANA, MUSCA DOMESTICA, BOMBYX MORI WHOLE, and AEDES TAENIORHYNCHUS
Dosage form
SOLUTION
Route
SUBLINGUAL
Labeler
DNA Labs, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1990-01-01
Substance
AEDES TAENIORHYNCHUS; BOMBYX MORI WHOLE; MUSCA DOMESTICA; PERIPLANETA AMERICANA; SOLENOPSIS INVICTA
Active strength
30; 30; 30; 30; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Ant Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Insect Proteins [CS], Insect Proteins [CS], Insect Proteins [CS], Insect Proteins [CS], Non-Standardized Insect Allergenic Extract [EPC], Non-Standardized Insect Allergenic Extract [EPC], Non-Standardized Insect Allergenic Extract [EPC], Non-Standardized Insect Venom Allergenic Extract [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termMatched term
BN2DNW66IQAEDES TAENIORHYNCHUSAEDES TAENIORHYNCHUS
6MT58Z9E5PBOMBYX MORI WHOLEBOMBYX MORI WHOLE
PV7823W303MUSCA DOMESTICAMUSCA DOMESTICA
2RQ1L9N089PERIPLANETA AMERICANAPERIPLANETA AMERICANA
5O7CR4P444SOLENOPSIS INVICTASOLENOPSIS INVICTA

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
58264-0311-15826403110129.57 mL in 1 BOTTLE, GLASS (58264-0311-1) 29.57 ml1990-01-01NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
A-19DNA Labs, Inc.2025-01-09HUMAN OTC DRUG LABEL3