Home NDC 73656-006 NDC 73656-006 - WHITE GLO BIO-ENZYME This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 73656-006
Package NDCs from labels 73656-006-00
Manufacturer WHITE GLO USA INC | Suzhou Baozi Healthy Technology Co.,Ltd
Effective date 2025-02-26
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73656-006 WHITE GLO BIO-ENZYME (SODIUM MONOFLUOROPHOSPHATE) KIT [WHITE GLO USA INC] 6 Unmatched 20250228_f894a841-0df7-470d-8fc2-c9d6ba0edf99.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 13 of 191 · 3,817 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join DRAVYNOR TOPICAL ANALGESIC HEAT Patch MENTHOL 24MG CAPSAICIN 16MG TOPICAL ANALGESIC HEAT PATCH Wenzhou Yuyuan Pharmaceutical Co., Ltd. 56b83ee8-8d86-9436-e063-6294a90a0c25 2026-07-16 Warnings Exact identifier unii: L7T10EIP3A OWELL NATURALS NEUROPATHY MAXIMUM STRENGTH MENTHOL OWELL NATURAL 8 LLC 56b8d0cc-2f35-7d38-e063-6294a90ad06d 2026-07-16 Warnings Exact identifier unii: L7T10EIP3A ANTIPHLAMINE L-MENTHOL, L-CAMPHOR, METHYL SALICYLATE Masaem Company 56b93c89-295b-f33a-e063-6294a90a5fe4 2026-07-16 Warnings Exact identifier unii: LAV5U5022Y Medicated Chest Rub CAMPHOR, EUCALYPTUS OIL, MENTHOL Old East Main Co. 7855033e-6a12-4cd8-b0a2-c5d69018d117 2026-07-16 Warnings, Adverse reactions Exact identifier unii: L7T10EIP3A Meriwether Skin Pain Relief MENTHOL, UNSPECIFIED FORM Meriwether Skin LLC f6e155be-5879-4176-bb0e-e364f2e5cdf9 2026-07-16 Warnings Exact identifier unii: L7T10EIP3A Sanatos MENTHOL Pharmadel LLC 522e1e7f-98ed-c475-e063-6294a90a622c 2026-07-16 Warnings Exact identifier unii: L7T10EIP3A COLGATE KPOP DEMON HUNTERS BUBBLE POP SODIUM FLUORIDE Colgate-Palmolive Company bf465181-01e9-44ca-91f8-03110a606774 2026-07-16 Warnings Exact identifier application number: M021 Colgate Minions Mild Bubble Fruit Fluoride SODIUM FLUORIDE Colgate-Palmolive Company 16634b99-f305-48bf-ac54-a9f53797a9e5 2026-07-16 Warnings Exact identifier application number: M021 Medi-First Muscle Rub Cream MENTHOL, METHYL SALICYLATE Unifirst First Aid Corporation 56a6b8b2-7ab0-9854-e063-6294a90ab5ba 2026-07-15 Warnings Exact identifier unii: L7T10EIP3A unii: LAV5U5022Y Freshen Up Holiday mint SODIUM FLUORIDE Dabur India Limited 56aaa9f5-7eac-11d9-e063-6294a90af3a8 2026-07-15 Warnings Exact identifier application number: M021 Freshen Up pepper mint SODIUM FLUORIDE Dabur India Limited 56aaba60-523e-6ac7-e063-6394a90a2756 2026-07-15 Warnings Exact identifier application number: M021 Freshen-up Matcha Mint SODIUM FLUORIDE Dabur India Limited 56aac050-73e7-298c-e063-6294a90a26eb 2026-07-15 Warnings Exact identifier application number: M021 Freshen Up twisted peppermint SODIUM FLUORIDE Dabur India Limited 56aac7a7-c086-2fa5-e063-6294a90aa959 2026-07-15 Warnings Exact identifier application number: M021 Freshen Up Vanilla Mint SODIUM FLUORIDE Dabur India Limited 56aad223-db88-7cf6-e063-6394a90a6b72 2026-07-15 Warnings Exact identifier application number: M021 Freshen Up SODIUM FLUORIDE MKJ BRANDS LLC 2dcd4816-caa5-c006-e063-6394a90ac487 2026-07-15 Warnings Exact identifier application number: M021 Freshen Up SODIUM FLUORIDE DABUR INDIA LIMITED 56acecd2-6966-2ee4-e063-6394a90a356f 2026-07-15 Warnings Exact identifier application number: M021 Colgate Max Fresh Advanced Whitening SODIUM FLUORIDE Colgate-Palmolive Company 01c07c25-2748-4d90-9505-094e2c977c9c 2026-07-15 Warnings Exact identifier application number: M021 VARICOSE VEINS MAXIMUM STRENGTH MENTHOL OWELL NATURAL & LLC 5692914f-1b14-e3e3-e063-6394a90a94bf 2026-07-14 Warnings Exact identifier unii: L7T10EIP3A Crest Strawberry SODIUM FLUORIDE The Procter & Gamble Manufacturing Company 7d51c67b-7409-e5a7-e053-2a91aa0a81fa 2026-07-14 Warnings Exact identifier application number: M021 Freshen Up SODIUM FLUORIDE, POTASSIUM NITRATE MKJ BRANDS LLC 476f453b-9215-0a11-e063-6294a90a5cd4 2026-07-14 Warnings Exact identifier application number: M021 rxcui: 545626 unii: C810JCZ56Q
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.