MedPath

Tiger Supply Inc APF

Approved
Approval ID

852de04d-f608-4f7f-b76b-25a29967c090

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jan 20, 2022

Manufacturers
FDA

Tiger Supply Inc

DUNS: 168720709

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Sodium Fluoride

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code69484-056
Product Classification
G
Generic Name
Sodium Fluoride
Product Specifications
Route of AdministrationDENTAL
Effective DateJanuary 20, 2022
FDA Product Classification

INGREDIENTS (12)

CITRIC ACID MONOHYDRATEInactive
Code: 2968PHW8QP
Classification: IACT
PHOSPHORIC ACIDInactive
Code: E4GA8884NN
Classification: IACT
MAGNESIUM ALUMINUM SILICATEInactive
Code: 6M3P64V0NC
Classification: IACT
POLYSORBATE 20Inactive
Code: 7T1F30V5YH
Classification: IACT
SACCHARIN SODIUMInactive
Code: SB8ZUX40TY
Classification: IACT
SODIUM BENZOATEInactive
Code: OJ245FE5EU
Classification: IACT
XYLITOLInactive
Code: VCQ006KQ1E
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
XANTHAN GUMInactive
Code: TTV12P4NEE
Classification: IACT
FD&C BLUE NO. 1Inactive
Code: H3R47K3TBD
Classification: IACT
SODIUM FLUORIDEActive
Quantity: 5.6 g in 454 g
Code: 8ZYQ1474W7
Classification: ACTIM

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Tiger Supply Inc APF - FDA Drug Approval Details