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FDA Approval

MILK OF MAGNESIA CHERRY

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

FDA Approval Summary

Company
Effective Date
March 31, 2025
Labeling Type
HUMAN OTC DRUG LABEL
Magnesium hydroxide(1200 mg in 15 mL)

Registrants1

Companies and organizations registered with the FDA for this drug approval, including their contact information and regulatory details.

GCP Laboratories

965480861

Manufacturing Establishments1

FDA-registered manufacturing facilities and establishments involved in the production, packaging, or distribution of this drug product.

GCP LABORATORIES

Geri-Care Pharmaceuticals, Corp

GCP Laboratories

965480861

Products1

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

MILK OF MAGNESIA CHERRY

Product Details

NDC Product Code
57896-001
Application Number
M007
Marketing Category
OTC Monograph Drug (C200263)
Route of Administration
ORAL
Effective Date
March 31, 2025
CITRIC ACID MONOHYDRATEInactive
Code: 2968PHW8QPClass: IACT
D&C RED NO. 28Inactive
Code: 767IP0Y5NHClass: IACT
GLYCERINInactive
Code: PDC6A3C0OXClass: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61UClass: IACT
SUCROSEInactive
Code: C151H8M554Class: IACT
XANTHAN GUMInactive
Code: TTV12P4NEEClass: IACT
Code: NBZ3QY004SClass: ACTIBQuantity: 1200 mg in 15 mL
WATERInactive
Code: 059QF0KO0RClass: IACT
SODIUM CITRATEInactive
Code: 1Q73Q2JULRClass: IACT
SODIUM HYPOCHLORITEInactive
Code: DY38VHM5ODClass: IACT
CARBOXYMETHYLCELLULOSE SODIUMInactive
Code: K679OBS311Class: IACT
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