Active Ingredient (In Each Teaspoonful (5 Ml))
Diphenhydramine HCl 12.5 mg
The following Structured Product Label (SPL) was submitted to the FDA by Akron Pharma Inc. for the product Diphenhydramine Hcl (NDC 71399-0125). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (in each teaspoonful (5 ml)), purpose, uses, do not use, ask a doctor before use if you have, ask a doctor or pharmacist before use if you are, when using this product, if pregnant or breast-feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Diphenhydramine HCl 12.5 mg
Antihistamine
taking sedatives or tranquilizers.
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
| Age | Dose |
| adults and children 12 years and over | 2 - 4 teaspoonsful (25 mg to 50 mg) |
| children 6 to 11 years | 1 - 2 teaspoonsful (12.5 mg to 25 mg) |
| children 2 to 5 years | do not use unless directed by a doctor |
| children under 2 years | do not use |
Bubble Gum Flavor, Citric Acid, Purified Water, Sodium Benzoate, Sodium Citrate, Sodium Saccharin, Sorbitol Solution 70% & Sucrose.
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Manufactured for:
Akron Pharma, Inc,
Fairfield, NJ 07004
Manufactured in U.S.A
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