Label: ALLERGY ATTACK RELIEF TO GO- diphenhydramine hydrochloride powder
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Contains inactivated NDC Code(s)
NDC Code(s): 51596-009-01, 51596-009-05, 51596-009-10, 51596-009-12, view more51596-009-24 - Packager: Breakthrough Products Inc.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated October 9, 2014
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (per powder)
- Purpose
- Uses
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Warnings
Ask a doctor before use if you have
- glaucoma
- a breathing problem such as emphysema or chronic bronchitis
- trouble urinating due to an enlarged prostate gland
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Directions
adults and children 12 years and over:
- see instructions in red box for opening packet
- place 25mg (1 powder) to 50mg (2 powders) on the tongue and swallow with or without water
- take every 4 to 6 hours
- do not take more than 300mg (12 powders) in 24 hours
children 6 to under 12 years of age:
- place 12.5mg (this dose strength is not available in this package) to 25mg (1 powder) on the tongue and swallow with or without water
- take every 4 to 6 hours
- do not take more than 150mg (6 powders) in 24 hours
- do not attempt to divide a powder in half
children under 6 years of age: do not use
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 1 Powder Packet
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INGREDIENTS AND APPEARANCE
ALLERGY ATTACK RELIEF TO GO
diphenhydramine hydrochloride powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51596-009 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 25 mg Inactive Ingredients Ingredient Name Strength anhydrous citric acid (UNII: XF417D3PSL) ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B) dextrose (UNII: IY9XDZ35W2) HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P) sucralose (UNII: 96K6UQ3ZD4) sucrose (UNII: C151H8M554) Product Characteristics Color WHITE Score Shape Size Flavor RASPBERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51596-009-10 10 in 1 BOX 1 1 in 1 PACKET; Type 0: Not a Combination Product 2 NDC:51596-009-05 5 in 1 BOX 2 NDC:51596-009-01 1 in 1 POUCH; Type 0: Not a Combination Product 3 NDC:51596-009-12 12 in 1 BOX 3 1 in 1 POUCH; Type 0: Not a Combination Product 4 NDC:51596-009-24 24 in 1 BOX 4 1 in 1 POUCH; Type 0: Not a Combination Product 5 NDC:51596-009-01 1 in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part341 10/01/2012 Labeler - Breakthrough Products Inc. (962008251)