Dynashield

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: Dynashield
Generic name: ZINC OXIDE
Manufacturer: Dynarex Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 59fd865c-b81d-43ad-8fa0-c37ca0557769
SPL ID: 4e3e4630-9843-775a-e063-6294a90a3ca0
Version: 10
Effective date: 2026-03-30
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:56:34

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 · 25 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		Dynashield	openfda.brand_name
generic name		ZINC OXIDE	openfda.generic_name
manufacturer name		Dynarex Corporation	openfda.manufacturer_name
ndc	package	67777-407-12	openfda.package_ndc
ndc	package	67777-407-13	openfda.package_ndc
ndc	package	67777-407-01	openfda.package_ndc
ndc	package	67777-407-02	openfda.package_ndc
ndc	package	67777-407-10	openfda.package_ndc
ndc	package	67777-407-11	openfda.package_ndc
ndc	package	67777-407-03	openfda.package_ndc
ndc	package	67777-407-04	openfda.package_ndc
ndc	product	67777-407	openfda.product_ndc
ndc11	package	67777040703	derived:openfda.package_ndc
ndc11	package	67777040701	derived:openfda.package_ndc
ndc11	package	67777040712	derived:openfda.package_ndc
ndc11	package	67777040704	derived:openfda.package_ndc
ndc11	package	67777040702	derived:openfda.package_ndc
ndc11	package	67777040711	derived:openfda.package_ndc
ndc11	package	67777040713	derived:openfda.package_ndc
ndc11	package	67777040710	derived:openfda.package_ndc
rxcui		1427410	openfda.rxcui
spl id		4e3e4630-9843-775a-e063-6294a90a3ca0	id
spl set id		59fd865c-b81d-43ad-8fa0-c37ca0557769	set_id
unii		SOI2LOH54Z	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 For External Use Only When using this product • Do not get into eyes Stop use and ask a doctor if: • Condition worsens • Symptoms last more than 7 days or clear up and occur again within a few days If pregnant or beast-feeding, ask a health professional before use Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away

Reported adverse events (FAERS/openFDA)#

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