FDA.report

Tampax

Primary DI
40073010022339
Brand
Tampax
Company
PROCTER & GAMBLE MANUFACTURING COMPANY, THE
Model
Tampax Pocket Pearl
Device description
TAMPAX POCKET PEARL REGULAR 36 CT
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
10073010022338PackageGS116In Commercial Distribution
40073010022339PackageGS140In Commercial Distribution
00073010022331PrimaryGS10
50073010022336Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
1007301002233810073010022338
4007301002233940073010022339
00073010022331000730100223310730100223310073010022331
5007301002233650073010022336

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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