FDA.report

Tampax

Primary DI
00001490839392
Brand
Tampax
Company
PROCTER & GAMBLE MANUFACTURING COMPANY, THE
Model
Tampax
Device description
TAMPAX OEF TRIPLEPACK LIGHTS-REGULAR-SUPER 36CT
Published
2016-09-15
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
true
Sterile
false
Single use
true

Related Records

Product Codes

CodeName
HEBTAMPON, MENSTRUAL, UNSCENTED

Product Code Classifications

CodeDeviceSpecialtyClass
HEBTampon, Menstrual, UnscentedObstetrics/Gynecology2

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00001490839392PackageGS184In Commercial Distribution
00073010000803PackageGS16In Commercial Distribution
00073010506022PrimaryGS10
50073010506027Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
00001490839392000014908393920014908393920001490839392
00073010000803000730100008030730100008030073010000803
00073010506022000730105060220730105060220073010506022
5007301050602750073010506027

GMDN Terms

TermDefinition
Menstrual tampon, unscentedA non-sterile, non-deodorized plug made of cellulosic or synthetic material that is inserted into the vagina to absorb menstrual or other vaginal discharge. This is a single-use device.

Sterilization Methods

Method

Regulatory Flags

DUNS number
004238200
Device count
36
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

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