Hydrate 1

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: Hydrate 1
Generic name: BERBERISAQUI,BETAVULGARIS,BOLDO,CARDUUSMARIANUS,CHELIDONIUMMAJUS,ELEUTHEROCOCCUS SENTICOSUS,HORDEUMVULGARE,IRISVERSICOLOR,ROSMARINUSOFFICINALIS,TARAXACUMOFFICINALE,XANTHOXYLUMFRAXINEUM,ULMUSFULVA,GLYCYRRHIZAGLABRA,GETTYSBURGAQUA,WILDBADAQUA,CARLSBADAQUA,ATP,NATRUMMURIATICUM,OXYGEN,SILICEA,WIESBADENAQUA,HYDROGEN
Manufacturer: Natural Creations, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 189bc53c-5d75-48df-a74e-cfff2d08d3a9
SPL ID: fa82372b-e2ff-4f58-bb8b-3b80acc432fb
Version: 2
Effective date: 2025-12-16
Source export date: 2026-09-28
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:08:23

Harmonized routes table
Harmonized routes
ORAL

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 · 26 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Hydrate 1	openfda.brand_name
generic name		BERBERISAQUI,BETAVULGARIS,BOLDO,CARDUUSMARIANUS,CHELIDONIUMMAJUS,ELEUTHEROCOCCUS SENTICOSUS,HORDEUMVULGARE,IRISVERSICOLOR,ROSMARINUSOFFICINALIS,TARAXACUMOFFICINALE,XANTHOXYLUMFRAXINEUM,ULMUSFULVA,GLYCYRRHIZAGLABRA,GETTYSBURGAQUA,WILDBADAQUA,CARLSBADAQUA,ATP,NATRUMMURIATICUM,OXYGEN,SILICEA,WIESBADENAQUA,HYDROGEN	openfda.generic_name
manufacturer name		Natural Creations, Inc	openfda.manufacturer_name
ndc	package	43406-0715-2	openfda.package_ndc
ndc	product	43406-0715	openfda.product_ndc
ndc11	package	43406071502	derived:openfda.package_ndc
spl id		fa82372b-e2ff-4f58-bb8b-3b80acc432fb	id
spl set id		189bc53c-5d75-48df-a74e-cfff2d08d3a9	set_id
unii		7E889U5RNN	openfda.unii
unii		2788Z9758H	openfda.unii
unii		A4KL1HMZ7T	openfda.unii
unii		7YNJ3PO35Z	openfda.unii
unii		4G174V5051	openfda.unii
unii		VZJ9F3C3SB	openfda.unii
unii		8JM482TI79	openfda.unii
unii		39981FM375	openfda.unii
unii		U946SH95EE	openfda.unii
unii		8L70Q75FXE	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		Q4EWM09M3O	openfda.unii
unii		S88TT14065	openfda.unii
unii		8JBE478M5Q	openfda.unii
unii		91QY4PXU8Q	openfda.unii
unii		X43D4L3DQC	openfda.unii
unii		ZX5Z2LW23O	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: Consult a physician for use in children under 12 years of age. IF PREGNANT OR BREAST-FEEDING , ask a health care professional before use. KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away. Do not use if TAMPER EVIDENT seal is broken or missing.

Reported adverse events (FAERS/openFDA)#

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