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Approvals
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Philippines FDA
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SHELOGEL
Approved
STANDARD
SHELOGEL
SCHEELE LABORATORIES PHIL. INC.
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
711d95d26345a618
Company
SCHEELE LABORATORIES PHIL. INC.
Type
Standard
Approval Details
Approval Id
711d95d26345a618
Drug Approval Philippines Name
SHELOGEL
Product Name
SHELOGEL
Registration Number
DRHR-1803
Brand Name
SHELOGEL
Generic Name
ALUMINUM HYDROXIDE + MAGNESIUM HYDROXIDE
Dosage Form
ORAL SUSPENSION
Dosage Strength
225mg/ 200mg per 5mL
Manufacturer
SCHEELE LABORATORIES PHIL. INC.
Issuance Date
28 November 2022
Expiry Date
03 October 2027
Pharmacologic Category
Antacid
Classification
Household Remedy (HR)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
711d95d26345a618
Type
Standard
Back to Philippines FDA Approvals
SHELOGEL - Philippines FDA Drug Approval Details