White Tetterine

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: White Tetterine
Generic name: MICONAZOLE NITRATE
Manufacturer: S.S.S. Company
Product type: HUMAN OTC DRUG
SPL set ID: 861895df-c989-4afd-bb31-c87c644139ef
SPL ID: 47e0c77d-9b4e-5d5f-e063-6294a90ae335
Version: 6
Effective date: 2026-01-08
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:38:51

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M005	openfda.application_number
brand name		White Tetterine	openfda.brand_name
generic name		MICONAZOLE NITRATE	openfda.generic_name
manufacturer name		S.S.S. Company	openfda.manufacturer_name
ndc	package	12258-242-01	openfda.package_ndc
ndc	product	12258-242	openfda.product_ndc
ndc11	package	12258024201	derived:openfda.package_ndc
rxcui		998458	openfda.rxcui
rxcui		998442	openfda.rxcui
spl id		47e0c77d-9b4e-5d5f-e063-6294a90ae335	id
spl set id		861895df-c989-4afd-bb31-c87c644139ef	set_id
unii		VW4H1CYW1K	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Do not use on children under 2 years of age unless directed by a doctor Do not use on diaper rash For external use only Stop use and ask a doctor if for athlete's foot and ringworm, irritation occurs or if there is no improvement within 4 weeks for jock itch if irritation occurs of if there is no improvement with-in 2 weeks When using this product Avoid contact with eyes KEEP OUT OF REACH OF CHILDREN If swallowed, get medical help or contact a Poison Control Center right away

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.