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PLANTSCRIPTION ANTI-AGING BROAD SPECTRUM SPF 25 - 59427-006-01 - (AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, and OXYBENZONE)

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Drug Information of PLANTSCRIPTION ANTI-AGING BROAD SPECTRUM SPF 25

Product NDC: 59427-006
Proprietary Name: PLANTSCRIPTION ANTI-AGING BROAD SPECTRUM SPF 25
Non Proprietary Name: AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, and OXYBENZONE
Active Ingredient(s): .02; .05; .075; .05; .03    g/mL; g/mL; g/mL; g/mL; g/mL & nbsp;   AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, and OXYBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of PLANTSCRIPTION ANTI-AGING BROAD SPECTRUM SPF 25

Product NDC: 59427-006
Labeler Name: ORIGINS NATURAL RESOURCES INC.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20121101

Package Information of PLANTSCRIPTION ANTI-AGING BROAD SPECTRUM SPF 25

Package NDC: 59427-006-01
Package Description: 1 JAR in 1 CARTON (59427-006-01) > 50 mL in 1 JAR

NDC Information of PLANTSCRIPTION ANTI-AGING BROAD SPECTRUM SPF 25

NDC Code 59427-006-01
Proprietary Name PLANTSCRIPTION ANTI-AGING BROAD SPECTRUM SPF 25
Package Description 1 JAR in 1 CARTON (59427-006-01) > 50 mL in 1 JAR
Product NDC 59427-006
Product Type Name HUMAN OTC DRUG
Non Proprietary Name AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, and OXYBENZONE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20121101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name ORIGINS NATURAL RESOURCES INC.
Substance Name AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE
Strength Number .02; .05; .075; .05; .03
Strength Unit g/mL; g/mL; g/mL; g/mL; g/mL
Pharmaceutical Classes

Complete Information of PLANTSCRIPTION ANTI-AGING BROAD SPECTRUM SPF 25


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