rexall travel toothbrush and tooth-paste
Generic: sodium monofluorophosphate
Labeler: old east main co.Drug Facts
Product Profile
Brand Name
rexall travel toothbrush and tooth-paste
Generic Name
sodium monofluorophosphate
Labeler
old east main co.
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
55910-087
Product ID
55910-087_6b3f8169-e476-425b-a9c8-f28b1cf6aadd
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2026-12-31
Marketing Start
2022-10-12
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55910087
Hyphenated Format
55910-087
Supplemental Identifiers
RxCUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
rexall travel toothbrush and tooth-paste (source: ndc)
Generic Name
sodium monofluorophosphate (source: ndc)
Application Number
M021 (source: ndc)
Resolved Composition
Strengths
- 0.76 %
- 0.13 %
Packaging
- 1 KIT in 1 KIT (55910-087-01) * 24 g in 1 TUBE
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "6b3f8169-e476-425b-a9c8-f28b1cf6aadd", "openfda": {"rxcui": ["545626"], "spl_set_id": ["1bfba18b-1418-4c39-b666-96fa0674cc70"], "manufacturer_name": ["Old East Main CO."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (55910-087-01) * 24 g in 1 TUBE", "package_ndc": "55910-087-01", "marketing_start_date": "20221012"}], "brand_name": "Rexall Travel Toothbrush and Tooth-paste", "product_id": "55910-087_6b3f8169-e476-425b-a9c8-f28b1cf6aadd", "dosage_form": "KIT", "product_ndc": "55910-087", "generic_name": "Sodium monofluorophosphate", "labeler_name": "Old East Main CO.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Rexall Travel Toothbrush and Tooth-paste", "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221012", "listing_expiration_date": "20261231"}