Label: DICLOFENAC SODIUM- 3% diclofenac spray aerosol, metered
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Contains inactivated NDC Code(s)
NDC Code(s): 69621-300-01 - Packager: Shoreline Pharmaceuticals, Inc.
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated March 10, 2016
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- Official Label (Printer Friendly)
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GENERAL PRECAUTIONS
Diclofenac sodium 3% spray
Use as directed.
Qty 118
No refills
Shoreline Pharmaceuticals, Inc.
16530 Ventura Blvd, Suite 610
Encino, CA 91436
310.464.9170
Rx 616194
N Dr:
Date
Discard by
For External Use Only
Compounded by Shoreline Pharmaceuticals
Toll Free: 877-817-1885
You may report side effects to FDA at 1-800-FDA-1088
- NDC69621-300-10
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INGREDIENTS AND APPEARANCE
DICLOFENAC SODIUM
3% diclofenac spray aerosol, meteredProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:69621-300 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DICLOFENAC SODIUM (UNII: QTG126297Q) (DICLOFENAC - UNII:144O8QL0L1) DICLOFENAC SODIUM 30 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69621-300-01 1 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/07/2016 Labeler - Shoreline Pharmaceuticals, Inc. (078542781)
