Home FDA labels 0b1dae4a-5af6-4f34-804b-8a50f61b8c5a Buffer pH 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 Buffer pH
Generic name CHAMOMILLA, GRAPHITES, KALI CARBONICUM, KALI OXALICUM, KALI PHOSPHORICUM, MAGNESIA PHOSPHORICA, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NATRUM SULPHURICUM, NUX VOMICA, RHEUM (PALMATUM), ROBINIA PSEUDOACACIA
Manufacturer NaturalCare
Product type HUMAN OTC DRUG
SPL set ID 2161a2e2-613d-4dac-a5f6-796d40e849d9
SPL ID 0b1dae4a-5af6-4f34-804b-8a50f61b8c5a
Version 1
Effective date 2026-03-25
Source export date 2026-10-12
Source partition 4
Source file https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:39:34 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 · 20 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Buffer pH openfda.brand_name generic name CHAMOMILLA, GRAPHITES, KALI CARBONICUM, KALI OXALICUM, KALI PHOSPHORICUM, MAGNESIA PHOSPHORICA, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NATRUM SULPHURICUM, NUX VOMICA, RHEUM (PALMATUM), ROBINIA PSEUDOACACIA openfda.generic_name manufacturer name NaturalCare openfda.manufacturer_name ndc package 70163-0043-1 openfda.package_ndc ndc product 70163-0043 openfda.product_ndc ndc11 package 70163004301 derived:openfda.package_ndc spl id 0b1dae4a-5af6-4f34-804b-8a50f61b8c5a id spl set id 2161a2e2-613d-4dac-a5f6-796d40e849d9 set_id unii CI71S98N1Z openfda.unii unii 269XH13919 openfda.unii unii LC7F2W7I5B openfda.unii unii 4QQN74LH4O openfda.unii unii 0YPR65R21J openfda.unii unii G025DAL7CE openfda.unii unii HF539G9L3Q openfda.unii unii 451W47IQ8X openfda.unii unii BQN1B9B9HA openfda.unii unii G0R4UBI2ZZ openfda.unii unii 7TPC058OWY openfda.unii unii 70WT22SF4B 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: Stop use and ask a doctor if ■ symptoms worsen or persist for more than 14 days ■ new symptoms appear If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if printed foil blister is broken or missing. ■ Store at room temperature (65-80ºF)
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.